Publications by the Studer Group...
© Uni MS - AK Studer (photo: lt)

Studer Group Publications  (chronological order).

Photos

studer_publ_cover_gallery_2023_04
studer_publ_cover_gallery_2023_04
© Uni MS / AKS (lt)
  • P. Gerdt, A. Studer Angew. Chem. Int. Ed. 2022, 61, e202283961. [doi:10.1002/anie.202206964]
    © Wiley (Publisher), P. Gerdt (Idea), P. Gerdt, D. Leifert (Artwork)
  • N. L. Frye, C. G. Daniliuc, A. Studer, Angew. Chem. Int. Ed. 2022, 61, e202115593. [doi:10.1002/anie.202115593]
    © Wiley (Publisher), A. Studer, N. L. Frye (Idea), N. L. Frye (Artwork)
  • C. Gerleve, A. Studer,Angew. Chem. Int. Ed. 2020, 59, 15468-15473. [doi:10.1002/anie.202002595]
    © Wiley (Publisher), D. Leifert (Idea), D.Leifert (Artwork)
  • Special Issue: Radical Chemistry and Organic Synthesis , Adv. Synth. Catal. 2020, 362, 2071-2284.
    © Wiley (Publisher), D. Leifert, A. Studer (Idea), D. Leifert (Artwork)
  • D. Leifert, A. Studer, Angew. Chem. Int. Ed. 2020, 59, 74-108. [doi:10.1002/anie.201903726]
    © Wiley (Publisher), D. Leifert (Idea), D. Leifert (Artwork)
  • W. C. de Vries, S. Kudruk, D. Grill, M. Niehues, A. L. L. Matos, M. Wissing, A. Studer, V. Gerke, B. J. Ravoo, Adv. Sci. 2019, 6, 1901935. [doi:10.1002/advs.201901935]
    © Wiley (Publisher)
  • M. Wissing, A. Studer,Chem. Eur. J. 2019, 25, 5870-5874. [doi:10.1002/chem.201900493]
    © Wiley (Publisher), L. Tebben (Idea), L. Tebben (Artwork)
  • L. Liu, H. Klaasen, A. Timmer, H.-Y. Gao, D. Barton, H. Mönig, J. Neugebauer, H. Fuchs, A. Studer,J. Am. Chem. Soc. 2018, 140, 6000-6005. [doi:10.1021/jacs.8b02599]
    © ACS (Publisher), A. Studer (Idea), L. Tebben (Artwork)
  • Y. Cheng, C. Mück-Lichtenfeld, A. Studer,Angew. Chem. Int. Ed. 2018, 57, 16832-16836. [doi:10.1002/anie.201810782]
    © Wiley (Publisher), L. Tebben (Idea), L. Tebben (Artwork)
  • W. C. de Vries, D. Grill, M. Tesch, A. Ricker, H. Nüsse, J. Klingauf, A. Studer, V. Gerke, B. J. Ravoo, Angew. Chem. Int. Ed. 2017, 56, 9603-9607.
    [doi:10.1002/anie.201702620]
    © Wiley (Publisher), B. J. Ravoo, W. de Vries (Idea), W. de Vries (Artwork)
  • S. Bera, C. G. Daniliuc, A. Studer, Angew. Chem. Int. Ed. 2017, 56. [doi:10.1002/anie.201701485]
    © Wiley (Publisher), A. Studer, L. Tebben (Idea), L. Tebben (Artwork)
  • L. Tebben, A. Studer, Chem. Eur. J. 2017, 23, 5857-5859. [doi:10.1002/chem.201700451]
    © © Wiley (Publisher), L. Tebben (Idea), L. Tebben (Artwork)
  • P. A. Held, H. Fuchs, A. Studer, Chem. Eur. J. 2017, 23, early view. [doi:10.1002/chem.201604047]
    © Wiley (Publisher), P. Held (Idea), L. Tebben (Artwork)
  • N. B. Heine, A. Studer, Macrom. Rapid Commun. 2016, 37, 1494-1498. [doi:10.1002/marc.201600254]
    © Wiley (Publisher), A. Studer, N. Heine (Idea), M. Tesch (Artwork)
  • A. Studer, D. P. Curran, Angew. Chem. Int. Ed. 2016, 55, 58-102.
    [doi:10.1002/anie.201505090]
    © Wiley (Publisher), A. Studer, L. Tebben (Idea), L. Tebben (Artwork)
  • F. Klotter, A. Studer, Angew. Chem. Int. Ed. 2015, 54, 8547-8550.
    [doi:10.1002/anie.201502595]
    © Wiley (Publisher), A. Studer, F. Klotter, L. Tebben (Idea), L. Tebben (Artwork)
  • T. Buscher, A. Barroso, C. Denz, A. Studer, Polym. Chem. 2015, 6, 4221-4229.
    [doi:10.1039/C5PY00425J]
    © RSC (Publisher), A. Studer, T. Buscher (Idea), T. Buscher (Artwork)
  • F. Klotter, A. Studer, Angew. Chem. Int. Ed. 2014, 53, 2473-2476.
    [doi:10.1002/anie.201310676]
    © Wiley (Publisher), L. Tebben, A. Studer (Idea), L. Tebben (Artwork)
  • Z. Zeng, D. Matuschek, A. Studer, C. Schwickert, R. Pöttgen, H. Eckert, Dalton Trans. 2013, 42, 8585-8596. [doi:10.1039/C3DT50627D ]
    © RSC (Publisher), C. Schwickert, H. Eckert (Idea), C. Schwickert (Artwork)
  • M. Becker, L. De Cola, A. Studer, J. Mater. Chem. C 2013, 1, 3287-3290.
    [doi:10.1039/C3TC30358F]
    © RSC (Publisher), M. Becker (Idea), M. Becker (Artwork)
  • H.-Y. Gao, H. Wagner, D. Zhong, J.-H. Franke, A. Studer, H. Fuchs, Angew. Chem. Int. Ed. 2013, 52, 4024-4028.
    [doi:10.1002/anie.201208597]
    © Wiley (Publisher), H.-Y. Gao, H. Wagner, L. Tebben, A. Studer, H. Fuchs (Idea), L. Tebben (Artwork)
  • Encyclopedia of Radicals in Chemistry, Biology and Materials,
    C. Chatgilialoglu, A. Studer (Eds.), Wiley 2012.
    [doi:10.1002/9781119953678]
    © Wiley (Publisher)
  • C.-M. Chou, I. Chatterjee, A. Studer, Angew. Chem. Int. Ed. 2011, 50, 8614-8617. [doi:10.1002/anie.201103450]
    © Wiley (Publisher), A. Studer, L. Tebben (Idea), L. Tebben (Artwork)
  • L. Tebben, A. Studer, Angew. Chem. Int. Ed. 2011, 50, 5034-5068.
    [doi:10.1002/anie.201002547]
    © Wiley (Publisher), L. Tebben, A. Studer (Idea), L. Tebben (Artwork)


Have some clicks through
Cover Artwork recently published
by the Studer Group...
Enjoy!
 

 

444.
meta-C-H Halogenation of pyridines, quinolines, and isoquinolines: meta-chlorination of 2-phenylpyridine ,
P. Xu, A. Studer,
Org. Synth. 2024, 101, 524-541. [doi:10.15227/orgsyn.101.0524]
443.
Oxygen-free alkene hydration using nitroarenes: Diastereoselective hydration of cholesteryl acetate,
J. Elfert, A. Bhunia, A. Studer,
Org. Synth. 2024, 101, 460-477. [doi:10.15227/orgsyn.101.0460]
442.
Sonochemical Nitroxide-Mediated Polymerization: Harnessing Sonochemistry for Polymer Synthesis,
C. Pauly, L. Schlichter, B. J. Ravoo, A. Studer,
Macromol. Rapid Commun. 2024, 45, 2400732. [doi:10.1002/marc.202400732]
441.
Formal meta-C–H-Fluorination of Pyridines and Isoquinolines through Dearomatized Oxazinopyridine Intermediates,
M. Haring, K. Balanna, Q. Cheng, J. Lammert, A. Studer,
J. Am. Chem. Soc. 2024, 146, 30758-30763. [doi:10.1021/jacs.4c11759]
440.
Formal [2σ + 2σ]-Cycloaddition of Aziridines with Bicyclo[1.1.0]butanes: Access to Enantiopure 2-Azabicyclo[3.1.1]heptane Derivatives,
S. Dutta, C. G. Daniliuc, C. Mück-Lichtenfeld, A. Studer,
J. Am. Chem. Soc. 2024, 146, 27204-27212. [doi:10.1021/jacs.4c11296]
439.
Photocatalytic PPh3-Mediated Synthesis of C3-Functionalized Indoles via Radical Annulation of Nitroarenes and Alkenes,
J. Zhang, C. Mück-Lichtenfeld, M. A. Wiethoff, A. Studer,
Angew. Chem. Int. Ed. 2024, 62, e202416726. [doi:10.1002/anie.202416726]
438.
Iron-catalyzed radical Markovnikov hydrohalogenation and hydroazidation of alkenes,
J. Elfert, N. L. Frye, I. Rempel, C. G. Daniliuc, A. Studer,
Nat. Commun. 2024, 15, 7230. [doi:10.1038/s41467-024-51706-x]
437.
Intermolecular radical oxyalkylation of arynes with alkenes and TEMPO ,
D. Bhattacharya, M. Scherübl, C. G. Daniliuc, A. Studer,
Chem. Sci. 2024, 15, 13712-13716. [doi:10.1039/D4SC04369C]
436.
Emerging Progress: Photochemical Transformation of Nitroso Compounds,
Z.-L. Chen, Q.-Q. Li, A. Studer, J. Xuan,
Sci. China Chem. 2024, 67, accepted. [doi:10.1007/s11426-024-2096-6]
435.
Intramolecular Radical Amidooxygenation of Alkenes for the Construction of Pyrrolidinones,
A. Maity, A. Studer,
Org. Lett. 2024, 26, 4784-4787. [doi:10.1021/acs.orglett.4c01607]
434.
Para-Selective Radical Alkylation of Pyridines with Diacyl Peroxides and Peresters ,
Z. Wang, P. Xu, A. Studer,
Org. Chem. Front. 2024, 11, 3849-3854. [doi:10.1039/D4QO00814F]
433.
Introduction of the difluoromethyl group at the meta- or para-position of pyridines through regioselectivity switch,
P. Xu, Z. Wang, S.-M. Guo, A. Studer,
Nat. Commun. 2024, 15, 4121. [doi:10.1038/s41467-024-48383-1]
432.
Thermal and photoinduced radical cascade annulation using aryl isonitriles: An approach to quinoline-derived benzophosphole oxides,
S. K. Banjare, L. Lezius, E. S. Horst, D. Leifert, C. G. Daniliuc, F. A. Alasmary, A. Studer,
Angew. Chem. Int. Ed. 2024, 62, e202404275. [doi:10.1002/anie.202404275]
431.
Meta-Selective Copper-Catalyzed C–H Arylation of Pyridines and Isoquinolines through Dearomatized Intermediates,
S.-M. Guo, P. Xu, A. Studer,
Angew. Chem. Int. Ed. 2024, 62, e202405385. [doi:10.1002/anie.202405385]
430.
Organic Donor-Acceptor Thermally Activated Delayed Fluorescence Photocatalysts in the Photoinduced Dehalogenation of Aryl Halides,
M. A. Bryden, E. Crovini, T. Comerford, A. Studer, E. Zysman-Colman,
Angew. Chem. Int. Ed. 2024, 62, e202405081. [doi:10.1002/anie.202405081]
429.
Skeletal editing of pyridines through atom-pair swap from CN to CC,
Q. Cheng, D. Bhattacharya, M. Haring, H. Cao, C. Mück-Lichtenfeld, A. Studer,
Nat. Chem. 2024, 16, 741-748. [doi:10.1038/s41557-023-01428-2]
428.
Borylative transition metal-free couplings of vinyl iodides with various nucleophiles, alkenes or alkynes,
G. Seidler, M. Schwenzer, F. Clausen, C. G. Daniliuc, A. Studer,
Chem. Sci. 2024, 15, 1672-1678. [doi:10.1039/D3SC06131K]
427.
Aminoacylation of Alkenes by Cooperative NHC and Photoredox Catalysis,
L. Lezius, J. Reimler, N. Döben, M. Hamm, C. G. Daniliuc, A. Studer,
Synlett 2024, 35, 445-450. [doi:10.1055/a-2145-8697]
 
426.
Benzoyldiisopropylchlorosilane: a visible light photocleavable alcohol protecting group,
F. Lind, K. Markelov, A. Studer,
Chem. Sci. 2023, 14, 12615-12620. [doi:10.1039/D3SC04975B];
included in 2023 most popular organic chemistry articles.
425.
Cooperative Photoredox and N-Heterocyclic Carbene Catalyzed Fluoroaroylation for the Synthesis of α-Trifluoromethyl-Substituted Ketones,
X. Yu, A. Maity, A. Studer,
Angew. Chem. Int. Ed. 2023, 62, e202310288. [doi:10.1002/anie.202310288]
424.
Access to Polyheterocyclic Compounds through Iron(II)-Mediated Radical Cascade Cyclization Utilizing 2-Ethynylbenzaldehydes and Aryl Isonitriles,
S. K. Banjare, D. Leifert, F. Weidlich, C. G. Daniliuc, F. A. Alasmary, A. Studer,
Org. Lett. 2023, 25, 6424-6428. [doi:10.1021/acs.orglett.3c02448]
423.
Organic Synthesis Using Nitroxides,
D. Leifert, A. Studer,
Chem. Rev. 2023, 123, 10302-10380. [doi:10.1021/acs.chemrev.3c00212]
422.
C–H Functionalization of Pyridines via Oxazino Pyridine Intermediates: Switching to para-Selectivity under Acidic Conditions,
H. Cao, D. Bhattacharya, Q. Cheng, A. Studer,
J. Am. Chem. Soc. 2023, 145, 15581-15588. [doi:10.1021/jacs.3c05242]
421.
Photocatalytic phosphine-mediated water activation for radical hydrogenation,
J. Zhang, C. Mück-Lichtenfeld, A. Studer,
Nature 2023, 619, 506-513. [doi:10.1038/s41586-023-06141-1];
highlighted in Synfacts 2023, 19(09), 0921;
highlighted in Sci. China Mater. 2023, 66(10), 4133-4134;
highlighted in Chem 2023, 9, 2361-2366.
420.
1,2-Aminoxyalkylation of Alkenes with Alkyl Iodides and TEMPONa through SET- and XAT-Processes,
A. Maity, A. Studer,
Chem. Sci. 2023, 14, 7675-7680. [doi:10.1039/D3SC02544F]
419.
Lewis Acid Catalyzed Formal (3+2)-Cycloaddition of Bicyclo[1.1.0]butanes with Ketenes,
N. Radhoff, C. G. Daniliuc, A. Studer,
Angew. Chem. Int. Ed. 2023, 62, e202304771. [doi:10.1002/anie.202304771]
418.
Regioselective Formal β-Allylation of Carbonyl Compounds Enabled by Cooperative Nickel and Photoredox Catalysis,
K. Liu, Z. Wang, A. N. Künzel, M. Layh, A. Studer,
Angew. Chem. Int. Ed. 2023, 62, e202303473. [doi:10.1002/anie.202303473]
417.
Intramolecular Radical Oxygen-Transfer Reactions Using Nitroarenes,
J. Elfert, A. Bhunia, C. G. Daniliuc, A. Studer,
ACS Catal. 2023, 13, 6704-6709. [doi:10.1021/acscatal.3c00958]
416.
Regiodivergent C−H Acylation of Arenes by Switching from Ionic to Radical Type Chemistry Using NHC-Catalysis,
J. Reimler, X.-Y. Yu, N. Spreckelmeyer, C. G. Daniliuc, A. Studer,
Angew. Chem. Int. Ed. 2023, 62, e202303222. [doi:10.1002/anie.202303222]
415.
Alkyl Radical Generation from Alkylboronic Pinacol Esters through Substitution with Aminyl Radicals,
Z. Wang, N. Wierich, J. Zhang, C. G. Daniliuc, A. Studer,
J. Am. Chem. Soc. 2023, 145, 8770-8775. [doi:10.1021/jacs.3c01129]
414.
Rhodium-Catalyzed Hydrosilylation of Alkenes with Acylhydrosilanes,
F. Lind, A. Studer,
Chem. Eur. J. 2023, 29, e202301120. [doi:10.1002/chem.202301120]
413.
Enantioselective Copper-Catalyzed Fukuyama Indole Synthesis from 2-Vinylphenyl Isocyanides,
T. Drennhaus, D. Leifert, J. Lammert, J. P. Drennhaus, K. Bergander, C. G. Daniliuc, A. Studer,
J. Am. Chem. Soc. 2023, 145, 8665-8676. [doi:10.1021/jacs.3c01667]
412.
meta-Selective C−H Functionalization of Pyridines,
H. Cao, Q. Cheng, A. Studer,
Angew. Chem. Int. Ed. 2023, 62, e202302941. [doi:10.1002/anie.202302941]
411.
Highly Selective On-Surface Reactions of Aryl Propiolic Acids via Decarboxylative Coupling,
H. Kong, L. Viergutz, L. Liu, A. Sandvoß, X. Peng, H. Klaasen, H. Fuchs, A. Studer,
Adv. Mater. 2023, 35, 2210997. [doi:10.1002/adma.202210997]
410.
Bis(arylsulfonyl) Peroxide-Mediated Difunctionalization of Cyclic Enol Ethers,
R. O. McCourt, A. Studer,
J. Org. Chem. 2023, 88, 1860-1864. [doi:10.1021/acs.joc.2c02541]
409.
Iodine-Induced Self-Assembly Structure Transition of Organic Molecules on the Ag(111) Surface,
Y. Wang, K. Ma, T. Zhang, P. A. Held, A. Studer, H. Fuchs, Z. Hu, Z. Sun, Y. Han, H.-Y. Gao,
J. Phys. Chem. C 2023, 127, 1381-1387. [doi:10.1021/acs.jpcc.2c06589]
 
408.
Radical and ionic meta-C–H functionalization of pyridines, quinolines, and isoquinolines,
H. Cao, Q. Cheng, A. Studer,
Science 2022, 378, 779-785. [doi:10.1126/science.ade6029];
highlighted in Synfacts 2023, 19(03), 0221.
407.
Visible-Light-Mediated Radical Silyl-Oximation of Activated Alkenes Using tert-Butyl Nitrite and Silanes,
S. Plöger, A. Studer,
Org. Lett. 2022, 24, 8568-8572. [doi:10.1021/acs.orglett.2c03644]
406.
Radical NHC Catalysis,
K. Liu, M. Schwenzer, A. Studer,
ACS Catal. 2022, 12, 11984-11999. [doi:10.1021/acscatal.2c03996]
405.
Synthesis of 5-Membered Ring Systems Bearing gem-Difluoroalkenyl and Monofluoroalkenyl Substituents via Radical β-Bromo Fragmentation,
P. Xu, C. G. Daniliuc, K. Bergander, C. Stein, A. Studer,
ACS Catal. 2022, 12, 11934-11941. [doi:10.1021/acscatal.2c03775]
404.
Oxy-Borylenes as Photoreductants: Synthesis and Application in Dehalogenation and Detosylation Reactions,
P. Lenz, R. Oshimizu, S. Klabunde, C. G. Daniliuc, C. Mück-Lichtenfeld, J. C. Tendyck, T. Mori, W. Uhl, M. R. Hansen, H. Eckert, S. Yamaguchi, A. Studer,
Angew. Chem. Int. Ed. 2022, 61, e202209391. [doi:10.1002/anie.202209391]
403.
Azodioxy Compounds as Precursors for C-Radicals and Their Application in Thermal Styrene Difunctionalization,
S. Plöger, C. Mück-Lichtenfeld, C. G. Daniliuc, A. Studer,
Chem. Sci. 2022, 13, 9749-9754. [doi:10.1039/D2SC03860A]
402.
Cooperative NHC/Photoredox Catalysis: Three Component Radical Coupling of AroylFluorides, Styrenes and Alcohols,
N. Döben, J. Reimler, A. Studer,
Adv. Synth. Catal. 2022, 364, 3348-3353. [doi:10.1002/adsc.202200574]
401.
Oxidative NHC-catalyzed Intramolecular Friedel-Crafts-Alkylation of Indoles for the Synthesis of Spirocyclic Indolenines,
C. B. J. Breuers, C. G. Daniliuc, A. Studer,
Org. Lett. 2022, 24, 5314-5318. [doi:10.1021/acs.orglett.2c01927]
400.
Cooperative triple catalysis enables regioirregular formal Mizoroki–Heck reactions,
K. Liu, D. Leifert, A. Studer,
Nat. Synth. 2022, 6, 565–575. [doi:10.1038/s44160-022-00101-9]
399.
Decatungstate-catalyzed radical disulfuration through direct C-H functionalization for the preparation of unsymmetrical disulfides,
J. Zhang, A. Studer,
Nat. Commun. 2022, 13, 3886. [doi:10.1038/s41467-022-31617-5];
highlighted on the Nat. Commun. webpage. For Open Access see
398.
Dearomatizing Cyclization of 2-Iodoindoles by Oxidative NHC Catalysis to Access Spirocyclic Indolenines and Oxindoles Bearing an All Carbon Quaternary Stereocenter,
C. B. J. Breuers, C. G. Daniliuc, A. Studer,
Org. Lett. 2022, 24, 4960-4964. [doi:10.1021/acs.orglett.2c01851]
397.
Formal β-C-H Arylation of Aldehydes and Ketones by Cooperative Nickel and Photoredox Catalysis,
K. Liu, A. Studer,
Angew. Chem. Int. Ed. 2022, 61, e202206533. [doi:10.1002/anie.202206533]
396.
1,4-Aryl migration in ketene-derived enolates by a polar-radical-crossover cascade,
N. Radhoff, A. Studer,
Nat. Commun. 2022, 13, 3083. [doi:10.1038/s41467-022-30817-3];
For Open Access see
395.
Alternating Terpolymers through Cyclopolymerization and Subsequent Orthogonal Functionalization,
P. Gerdt, A. Studer,
Angew. Chem. Int. Ed. 2022, 61, e202206964. [doi:10.1002/anie.202206964];
selected as Hot Paper.
394.
Aroyl Fluorides as Bifunctional Reagents for Dearomatizing Fluoroaroylation of Benzofurans,
X. Yu, Q.-Y. Meng, C. G. Daniliuc, A. Studer,
J. Am. Chem. Soc. 2022, 144, 7072-7079. [doi:10.1021/jacs.2c01735]
393.
Oxindole Synthesis via Polar Radical Crossover of Ketene derived Amide Enolates in a Formal [3+2] Cycloaddition,
N. Radhoff, A. Studer,
Chem. Sci. 2022, 13, 3875-3879. [doi:10.1039/D1SC07134C]
392.
Allylboronic Esters as Acceptors in Radical Addition, Boron 1,2-Migration, and Trapping Cascades,
K. Jana, A. Studer,
Org. Lett. 2022, 24, 1100-1104. [doi:10.1021/acs.orglett.2c00039]
391.
1,3-Oxyalkynylation of Aryl Cyclopropanes with Ethylnylbenziodoxolones Using Photoredox Catalysis,
Z. Zuo, A. Studer,
Org. Lett. 2022, 24, 949-954. [doi:10.1021/acs.orglett.1c04319]
390.
Radical 1-Fluorosulfonyl-2-alkynylation of Unactivated Alkenes,
N. L. Frye, C. G. Daniliuc, A. Studer,
Angew. Chem. Int. Ed. 2022, 61, e202115593. [doi:10.1002/anie.202115593];
selected as Hot Paper.
389.
2,3-Difunctionalized Indoles via Radical Acylation or Trifluoromethylation of ortho-Alkynylphenyl Isonitriles,
D. Leifert, F. Weidlich, F. Adler, C. G. Daniliuc, F. A. Adlasmary, A. Studer,
Org. Lett. 2022, 24, 284-288. [doi:10.1021/acs.orglett.1c03916]
 
388.
Three-Component 1,2-Carboamination of Vinyl Boronic Esters via Amidyl Radical Induced 1,2-Migration,
C. You, A. Studer,
Chem. Sci. 2021, 12, 15765-15769. [doi:10.1039/D1SC05811H ]
387.
Conformational evolution following the sequential molecular dehydrogenation of PMDI on a Cu(111) surface,
L. Liu, A. Timmer, E.Kolodzeiski, H.-Y. Gao, H. Mönig, H. Klaasen, X. Meng, J. Ren, A. Studer, S. Amirjalayer, H. Fuchs,
Nanoscale Adv. 2021, 3, 6373-6378. [doi:10.1039/D1NA00590A]
386.
Remote Radical Desaturation of Unactivated C−H Bonds in Amides,
Y. Xia, K. Jana, A. Studer,
Chem. Eur. J. 2021, 27, 16621-16625. [doi:10.1002/chem.202103509]
385.
Cooperative NHC/Photoredox Catalyzed Ring-Opening of Aryl Cyclopropanes to 1-Aroyloxylated-3-Acylated Alkanes,
Z. Zuo, C. G. Daniliuc, A. Studer,
Angew. Chem. Int. Ed. 2021, 60, 25252-25257. [doi:10.1002/anie.202110304]
384.
Transition-Metal-Free Intramolecular Radical Aminoboration of Unactivated Alkenes,
D. Zheng, K. Jana, F. A. Alasmary, C. G. Daniliuc, A. Studer,
Org. Lett. 2021, 23, 7688-7692. [doi:10.1021/acs.orglett.1c03024]
383.
Visible-light Mediated Tryptophan Modification in Oligopeptides Employing Acylsilanes,
J. Reimler, A. Studer,
Chem. Eur. J. 2021, 27, 15392-15395. [doi:10.1002/chem.202102749]
382.
Direct Access to α-Aminosilanes Enabled by Visible-Light-Mediated Multicomponent Radical Cross-Coupling,
X. Yu, C. G. Daniliuc, F. A. Alasmary, A. Studer,
Angew. Chem. Int. Ed. 2021, 60, 23335-23341. [doi:10.1002/anie.202109252]
381.
Regio- and Stereoselective 1,2-Carboboration of Ynamides with Aryldichloroboranes,
C. You, M. Sakai, C. G. Daniliuc, K. Bergander, S. Yamaguchi, A. Studer,
Angew. Chem. Int. Ed. 2021, 60, 21697-21701. [doi:10.1002/anie.202107647]
380.
Intramolecular Hydrogen Atom Transfer Induced 1,2-Migration of Boronate Complexes,
D. Wang, K. Jana, A. Studer,
Org. Lett. 2021, 23, 5879-5879. [doi:10.1021/acs.orglett.1c01998]
379.
Radical Aryl Migration from Boron to Carbon,
D. Wang, C. Mück-Lichtenfeld, C. G. Daniliuc, A. Studer,
J. Am. Chem. Soc. 2021, 143, 9320-9326. [doi:10.1021/jacs.1c04217]
378.
Photo Click Reaction of Acylsilanes with Indoles,
C. Stuckhardt, M. Wissing, A. Studer,
Angew. Chem. Int. Ed. 2021, 60, 18605-18611. [doi:10.1002/anie.202101689]
377.
Remote Site-selective Radical C(sp3)-H Monodeuteration of Amides using D2O,
L. Wang, Y. Xia, V. Derdau, A. Studer,
Angew. Chem. Int. Ed. 2021, 60, 18645-18650. [doi:10.1002/anie.202104254]
376.
Synthesis of Stannylated Aryl Imines and Amines via Aryne Insertion Reactions into Sn−N Bonds,
E. Kran, C. Mück-Lichtenfeld, C. G. Daniliuc, A. Studer,
Chem. Eur. J. 2021, 27, 9281-9285. [doi:10.1002/chem.202101124]
375.
Recent advances in radical chemistry proceeding through pro-aromatic radicals,
A. Bhunia, A. Studer,
Chem 2021, 7, 2060-2100. [doi:10.1016/j.chempr.2021.03.023]
374.
Three-Component Aminoarylation of Electron-Rich Alkenes by Merging Photoredox with Nickel Catalysis,
H. Jiang, X. Yu, C. G. Daniliuc, A. Studer,
Angew. Chem. Int. Ed. 2021, 60, 14399-14404. [doi:10.1002/anie.202101775]
373.
Benzylic C−H acylation by cooperative NHC and photoredox catalysis,
Q.-Y. Meng, L. Lezius, A. Studer,
Nat. Commun. 2021, 12, 2068. [doi:10.1038/s41467-021-22292-z];
highlighted in Synform 2021, 08, A136.
372.
Polymerization of silanes through dehydrogenative Si–Si bond formation on metal surfaces,
L. Liu, H. Klaasen, M. C. Witteler, B. Schulze Lammers, A. Timmer, H. Kong, H. Mönig, H.-Y. Gao, J. Neugebauer, H. Fuchs, A. Studer,
Nat. Chem. 2021, 13, 350-357. [doi:10.1038/s41557-021-00651-z]
371.
Direct α-Acylation of Alkenes via N-Heterocyclic Carbene, Sulfinate, and Photoredox Cooperative Triple Catalysis,
K. Liu, A. Studer,
J. Am. Chem. Soc. 2021, 143, 4903-4909. [doi:10.1021/jacs.1c01022]
370.
Synthesis of Polymers Bearing a Chiral Backbone via Stereospecific Ionic Ring-Opening Polymerization of Chiral Donor-Acceptor Cyclopropanes,
A. Emmerich, C. G. Daniliuc, A. Studer,
Macromol. Rapid. Commun. 2021, 42, 2100030. [doi:10.1002/marc.202100030]
369.
Photo-mediated Intermolecular Coupling of Alkenes with Ketones via Acyloxy Nitroso Compounds,
D. Zheng, S. Plöger, C. G. Daniliuc, A. Studer,
Angew. Chem. Int. Ed. 2021, 60, 8547-8551. [doi:10.1002/anie.202016955]
368.
Preparation of α-Perfluoroalkyl Ketones from α,β-unsaturated Ketones via formal Hydroperfluoroalkylation,
K. Jana, I. Mizota, A. Studer,
Org. Lett. 2021, 23, 1280-1284. [doi:10.1021/acs.orglett.0c04260]
367.
Fe-catalyzed anaerobic Mukaiyama-type hydration of alkenes using nitroarenes,
A. Bhunia, K. Bergander, C. G. Daniliuc, A. Studer,
Angew. Chem. Int. Ed. 2021, 60, 8313-8320. [doi:10.1002/anie.202015740];
highlighted in Synfacts 2021, 17(04), 0419.
366.
Electronic effects in profluorescent benzotriazinyl radicals: A combined experimental and theoretical study,
J. Exner, I. Maisuls, A. Massolle, S. Klabunde, M. R. Hansen, C. A. Strassert, J. Neugebauer, H. Eckert, A. Studer,
Phys. Chem. Chem. Phys. 2021, 23, 2999-3007. [doi:10.1039/D0CP05732K]
365.
Functionalization of α‐C(sp3)‒H Bonds in Amides Using Radical Translocating Arylating Groups,
N. Radhoff, A. Studer,
Angew. Chem. Int Ed. 2021, 60, 3561-3565. [doi:10.1002/anie.202013275];
highlighted in Synfacts 2021, 17(03), 0295.
364.
Azo bond formation on metal surfaces,
X. Meng, H. Klaasen, L. Viergutz, B. Schulze Lammers, M. C. Witteler, H. Mönig, S. Amirjalayer, L. Liu, J. Neugebauer, H.-Y. Gao, A. Studer, H. Fuchs,
Angew. Chem. Int. Ed. 2021, 60, 1458-1464. [doi:10.1002/anie.202011858]
363.
Arynes as Radical Acceptors: TEMPO‐mediated Cascades Comprising Addition, Cyclization and Trapping,
M. Scherübl, C. G. Daniliuc, A. Studer,
Angew. Chem. Int. Ed. 2021, 60, 711-715. [doi:10.1002/anie.202012654]
362.
1,1,2-Trifunctionalization of Terminal Alkynes by Radical Addition-Translocation-Cyclization-Trapping for the Construction of Highly Substituted Cyclopentanes,
Y. Yang, C. G. Daniliuc, A. Studer,
Angew. Chem. Int. Ed. 2021, 60, 2145-2148. [doi:10.1002/anie.202011785]
361.
Oligosilanes as Silyl Radical Precursors through Oxidative Si−Si Bond Cleavage using Redox Catalysis,
X. Yu, M. Lübbesmeyer, A. Studer,
Angew. Chem. Int. Ed. 2021, 60, 675-679. [doi:10.1002/anie.202011738]
 
360.
An oxo-verdazyl radical for a symmetrical non-aqueous redox flow battery,
A. Korshunov, M. J. Milner, M. Grünebaum, A. Studer, M. Winter, I. Cekic-Laskovic,
J. Mater. Chem. A 2020, 8, 22280-22291. [doi:10.1039/D0TA07891C]
359.
Total Synthesis of (+)-Galbulin and Unnatural Lignans,
F. Clausen, A. Studer,
Org. Lett. 2020, 22, 6780-6783. [doi:10.1021/acs.orglett.0c02294]
358.
Investigation of phase II metabolism of 11-hydroxy-Δ-9-tetrahydrocannabinol and metabolite verification by chemical synthesis of 11-hydroxy-Δ-9-tetrahydrocannabinol-glucuronide,
C. Hassenberg, F. Clausen, G. Hoffmann, A. Studer, J. Schürenkamp,
Int. J. Legal Med. 2020, 134, 2105-2119. [doi:10.1007/s00414-020-02387-w]
357.
Synthesis of Alkyl Silanes via Reaction of Unactivated Alkyl Chlorides and Triflates with Silyl Lithium Reagents,
S. Mallick, E.-U. Würthwein, A. Studer,
Org. Lett. 2020, 22, 6568-6572. [doi:10.1021/acs.orglett.0c02337]
356.
Aryl Triflates in On-Surface Chemistry,
J. Ren, H. Klaasen, M. C. Witteler, L. Viergutz, J. Neugebauer, H.-Y. Gao, A. Studer, H. Fuchs,
Chem. Eur. J. 2020, 26, 16727-16732. [doi:10.1002/chem.202002486]
355.
Cooperative NHC and Photoredox Catalysis for the Synthesis of β-Trifluoromethylated Alkyl Aryl Ketones,
Q.-Y. Meng, N. Döben, A. Studer,
Angew. Chem. Int. Ed. 2020, 59, 19956-19960. [doi:10.1002/anie.202008040];
highlighted in Synfacts 2020, 16(02), 1180.
354.
Synthesis of 1,3‐Bis‐(boryl)alkanes via Boronic Ester‐Induced Consecutive Double 1,2‐Migration,
C. You, A. Studer,
Angew. Chem. Int. Ed. 2020, 59, 17245-17249. [doi:10.1002/anie.202007541]
353.
Nickel-Catalyzed Markovnikov Transfer Hydrocyanation in the Absence of Lewis Acid,
N. L. Frye, A. Bhunia, A. Studer,
Org. Lett. 2020, 22, 4456-4460. [doi:10.1021/acs.orglett.0c01454]
352.
1,n-Bisborylalkanes via Radical Boron Migration,
D. Wang, C. Mück-Lichtenfeld, A. Studer,
J. Am. Chem. Soc. 2020, 142, 9119-9123. [doi:10.1021/jacs.0c03058]
351.
Synthesis and Immobilization of Metal Nanoparticles Using Photoactive Polymer‐Decorated Zeolite L Crystals and Their Application in Catalysis,
M. Wissing, M. Niehues, B. J. Ravoo, A. Studer,
Adv. Synth. Catal. 2020, 362, 2245-2253. [doi:10.1002/adsc.202000208]
350.
Transition-metal-free Oxidative Cross-Coupling of Tetraarylborates to Biaryls Using Organic Oxidants,
C. Gerleve, A. Studer,
Angew. Chem. Int. Ed. 2020, 59, 15468-15473. [doi:10.1002/anie.202002595];
selected as Hot Paper.
349.
Intermolecular Radical Carboamination of Alkenes,
H. Jiang, A. Studer,
Chem. Soc. Rev. 2020, 49, 1790-1811. [doi:10.1039/C9CS00692C]
348.
Synthesis of Difluoromethylated Allenes through Trifunctionalization of 1,3-Enynes,
M. Muhammad, Y. Jiao, C. Ye, M.-F. Chiou, M. Israr, X. Zhu, Y. Li, Z. Wen, A. Studer, H. Bao,
Nat. Commun. 2020, 11, 416. [doi:10.1038/s41467-019-14254-3]
347.
Radical 1,3-Difunctionalization of Allylboronic Esters with Concomitant 1,2-Boron Shift,
K. Jana, A. Bhunia, A. Studer,
Chem 2020, 6, 512-522. [doi:10.1016/j.chempr.2019.12.022]
346.
Base-promoted C-C bond activation enables radical allylation with homoallylic alcohols,
M. Lübbesmeyer, E. G. Mackay, M. A. R. Raycroft, J. Elfert, D. A. Pratt, A. Studer,
J. Am. Chem. Soc. 2020, 142, 2609-2616. [doi:10.1021/jacs.9b12343]
345.
Radical‐induced 1,2‐Migrations of Boron Ate Complexes,
M. Kischkewitz, F. W. Friese, A. Studer,
Adv. Synth. Catal. 2020, 362, 2077-2087. [doi:10.1002/adsc.201901503];
selected as Very Important Paper.
344.
A Benzophenone-based Photocaging Strategy for the N7 Position of Guanosine,
L. Anhäuser, N. Klöcker, F. Muttach, F. Mäsing, P. Spacek, A. Studer, A. Rentmeister,
Angew. Chem. Int. Ed. 2020, 59, 3161-3165. [doi:10.1002/anie.201914573]
343.
Mild C–F Activation in Perfluorinated Arenes through Photosensitized Insertion of Isonitriles at 350 nm,
F. Weidlich, N. Esumi, D. Chen, C. Mück-Lichtenfeld, E. Zysman-Colman, A. Studer,
Adv. Synth. Catal. 2020, 362, 376-383. [doi:10.1002/adsc.201901126]
342.
Reaction of Vinylaziridines with Arynes: Synthesis of Benzazepines and Branched Allyl Fluorides,
S. Kaldas, E. Kran, C. Mück-Lichtenfeld, A. K. Yudin, A. Studer,
Chem. Eur. J. 2020, 26, 1501-1505. [doi:10.1002/chem.201904727]
341.
The Persistent Radical Effect in Organic Synthesis,
D. Leifert, A. Studer,
Angew. Chem. Int. Ed. 2020, 59, 74-108. [doi:10.1002/anie.201903726]
 
340.
Controlled Cellular Delivery of Amphiphilic Cargo by Redox-Responsive Nanocontainers,
W. C. de Vries, S. Kudruk, D. Grill, M. Niehues, A. L. L. Matos, M. Wissing, A. Studer, V. Gerke, B. J. Ravoo,
Adv. Sci. 2019, 6, 1901935. [doi:10.1002/advs.201901935];
showcased as Inside Back Cover.
339.
Carboamination of Unactivated Alkenes through Three‐Component Radical Conjugate Addition,
H. Jiang, G. Seidler, A. Studer,
Angew. Chem. Int Ed. 2019, 58, 16528-16532. [doi:10.1002/anie.201910926];
selected as Hot Paper;
among the top 10% most downloaded papers.
338.
Asymmetric Synthesis of Heterocyclic γ‐Amino Acid and Diamine Derivatives by Three‐Component Radical Cascade Reactions,
D. Zheng, A. Studer,
Angew. Chem. Int. Ed. 2019, 58, 15803-15807. [doi:10.1002/anie.201908987];
among the top 10% most downloaded papers.
337.
New avenues for C–B bond formation via radical intermediates,
F. W. Friese, A. Studer,
Chem. Sci. 2019, 10, 8503-8518. [doi:10.1039/C9SC03765A]
336.
Intermolecular Coupling and Intramolecular Cyclization of Aryl Nitriles on Au(111),
H. Klaasen, L. Liu, H. Gao, L. Viergutz, P. Held, T. Knecht, X. Meng, M. C. Börner, D. Barton, S. Amirjalayer, J. Neugebauer, A. Studer, H. Fuchs,
Chem. Commun. 2019, 55, 11611-11614. [doi:10.1039/C9CC03418H]
335.
Hydrogen Atom Transfer Induced Boron Retaining Coupling of Organoboronic Esters and Organolithium Reagents,
D. Wang, C. Mück-Lichtenfeld, A. Studer,
J. Am. Chem. Soc. 2019, 141, 14126-14130. [doi:10.1021/jacs.9b07960]
334.
Catalytic Protodeboronation of Pinacol Boronic Esters: Formal Anti-Markovnikov Hydromethylation of Alkenes,
F. Clausen, M. Kischkewitz, K. Bergander, A. Studer,
Chem. Sci. 2019, 10, 6210-6214. [doi: 10.1039/C9SC02067E]
333.
Deoxygenative Borylation of Secondary and Tertiary Alcohols,
F. W. Friese, A. Studer,
Angew. Chem. Int. Ed. 2019, 58, 9561-9564. [doi:10.1002/anie.201904028];
among the top 10% most downloaded papers.
332.
Diversity-oriented Desulfonylative Functionalization of Alkyl Allyl Sulfones,
Y. Xia, A. Studer,
Angew. Chem. Int. Ed. 2019, 58, 9836-9840. [doi:10.1002/anie.201903668];
among the top 10% most downloaded papers.
331.
Photochemical preparation of gold nanoparticle decorated cyclodextrin vesicles with tailored plasmonic properties,
W. C. de Vries, M. Niehues, M. Wissing, T. Würthwein, F. Mäsing, C. Fallnich, A. Studer, B. J. Ravoo,
Nanoscale 2019, 11, 9384-9391. [doi:10.1039/C9NR02363A]
330.
Anti‐Markovnikov Radical Hydro‐ and Deuteroamidation of Unactivated Alkenes,
H. Jiang, A. Studer,
Chem. Eur. J. 2019, 25, 7105-7109. [doi:10.1002/chem.201901566]
329.
Palladium-Catalyzed Decarboxylative γ-Arylation for the Synthesis of Tetrasubstituted Chiral Allenes,
I. Scheipers, C. Mück-Lichtenfeld, A. Studer,
Angew. Chem. Int. Ed. 2019, 58, 6545-6548. [doi:10.1002/anie.201901848]
328.
Chemistry With N-Centered Radicals Generated by Single-Electron Transfer-Oxidation Using Photoredox Catalysis,
H. Jiang, A. Studer,
CCS Chem. 2019, 1, 38-49. [doi:10.31635/ccschem.019.20180026]
327.
Tuning the Selectivity of AuPd Nanoalloys towards Selective Dehydrogenative Alkyne Silylation,
M. Wissing, A. Studer,
Chem. Eur. J. 2019, 25, 5870-5874. [doi:10.1002/chem.201900493];
showcased as Inside Back Cover;
highlighted in Synfacts 2019, 15(07), 0785.
326.
Synthesis of Para (−)-Δ8-THC Triflate as a Building Block for the Preparation of THC Derivatives Bearing Different Side Chains,
G. Hoffmann, C. G. Daniliuc, A. Studer,
Org. Lett. 2019, 21, 563-566. [doi:10.1021/acs.orglett.8b03907]
325.
Photoonitiated Three-Component α-Perfluoroalkyl-β-heteroarylation of Unactivated Alkenes via Electron Catalysis,
D. Zheng, A. Studer,
Org. Lett. 2019, 21, 325-329. [doi:10.1021/acs.orglett.8b03849]
324.
Diamantane suspended single copper atoms,
H.-Y. Gao, M. Šekutor, L. Liu, A. Timmer, H. Schreyer, H. Moenig, S. Amirjalayer, N. A. Fokina, A. Studer, P. R. Schreiner, H. Fuchs,
J. Am. Chem. Soc. 2019, 141, 315-322. [doi:10.1021/jacs.8b10067]
323.
Transition-Metal-Free Three-Component Radical 1,2-Amidoalkynylation of Unactivated Alkenes,
H. Jiang, A. Studer,
Chem. Eur. J. 2019, 25, 516-520. [doi:10.1002/chem.201805490]
322.
Silyldefluorination of Fluoroarenes via Concerted Nucleophilic Aromatic Substitution,
S. Mallick, P. Xu, E.-U. Würthwein, A. Studer,
Angew. Chem. Int. Ed. 2019, 58, 283-287. [doi:10.1002/anie.201808646]
 
321.
Intermolecular Acetoxyaminoalkylation of α-Diazo Amides with (Diacetoxyiodo)benzene and Amines,
N. Döben, H. Yan, M. Kischkewitz, J. Mao, A. Studer,
Org. Lett. 2018, 20, 7933-7936. [doi:10.1021/acs.orglett.8b03504]
320.
Antiferromagnetic Ordering Based on Intermolecular London Dispersion Interactions in Amphiphilic TEMPO Ammonium Salts,
J. Exner, S. Eusterwiemann, O. Janka, C. Doerenkamp, A. Massolle, O. Nienhaus, C. G. Daniliuc, R. Pöttgen, J. Neugebauer, A. Studer, H. Eckert,
Phys. Chem. Chem. Phys. 2018, 20, 28979-28983. [doi:10.1039/C8CP05837G]
319.
Cooperative palladium/Lewis acid-catalyzed transfer hydro-cyanation of alkenes and alkynes using 1-methylcyclohexa-2,5-diene-1-carbonitrile,
A. Bhunia, K. Bergander, A. Studer,
J. Am. Chem. Soc. 2018, 140, 16353-16359. [doi:10.1021/jacs.8b10651];
highlighted in Synfacts 2019, 15(02), 0161.
318.
Metal-Free Radical Borylation of Alkyl and Aryl Iodides,
Y. Cheng, C. Mück-Lichtenfeld, A. Studer,
Angew. Chem. Int. Ed. 2018, 57, 16832-16836. [doi:10.1002/anie.201810782];
showcased as Inside Back Cover;
selected as Hot Paper.
317.
Remote Site-Specific Radical Alkynylation of Unactivated C-H Bonds,
L. Wang, Y. Xia, K. Bergander, A. Studer,
Org. Lett. 2018, 20, 5817-5820. [doi:10.1021/acs.orglett.8b02514]
316.
Ferro- or Antiferromagnetism? Heisenberg Chains in the Crystal Structures of Verdazyl Radicals,
S. Eusterwiemann, C. Doerenkamp, T. Dresselhaus, O. Janka, C. G. Daniliuc, R. Pöttgen, A. Studer, H. Eckert, J. Neugebauer,
Phys. Chem. Chem. Phys. 2018, 20, 22902-22908. [doi:10.1039/C8CP03332C]
315.
The Special Role of B(C6F5)3 in the Single Electron Reduction of Quinones by Radicals,
X. Tao, C. Gabriel Daniliuc, R. Knitsch, M. R. Hansen, H. Eckert, M. Lübbesmeyer, A. Studer, G. Kehr, G. Erker,
Chem. Sci. 2018, 9, 8011-8018. [doi:10.1039/C8SC03005G]
314.
Site-selective Radical Remote C‒H Functionalization of Unactivated C‒H Bonds in Amides with Sulfone Reagents,
Y. Xia, L. Wang, A. Studer,
Angew. Chem. Int. Ed. 2018, 57, 12940-12944. [doi:10.1002/anie.201807455]
313.
Reaction Selectivity in On-Surface Chemistry by Surface Coverage Control - Alkyne Dimerization versus Alkyne Trimerization,
H. Klaasen, L. Liu, X. Meng, P. A. Held, H.-Y. Gao, D. Barton, C. Mück-Lichtenfeld, J. Neugebauer, H. Fuchs, A. Studer,
Chem. Eur. J. 2018, 24, 15303-15308. [doi:10.1002/chem.201802848]
312.
Preparation of Alkyl Boronic Esters Using Radical-Polar Crossover Reactions of Vinylboron Ate Complexes,
M. Kischkewitz, A. Studer,
Org. Synth. 2018, 95, 205-217. [doi:10.15227/orgsyn.095.0205]
311.
Remote C-H Functionalization Using Radical Translocating Arylating Groups,
F. W. Friese, C. Mück-Lichtenfeld, A. Studer,
Nat. Commun. 2018, 9, 2808. [doi:10.1038/s41467-018-05193-6];
selected as Editors' Highlight article.
310.
Metall-Free Direct C-H Cyanation of Alkenes,
X. Wang, A. Studer,
Angew. Chem. Int. Ed. 2018, 57, 11792-11796. [doi:10.1002/anie.201807303]
309.
Radical-Polar Crossover Reactions of Dienylboronate Complexes: Synthesis of Functionalized Allylboronic Esters,
M. Kischkewitz, C. Gerleve, A. Studer,
Org. Lett. 2018, 20, 3666-3669. [doi:10.1021/acs.orglett.8b01459]
308.
Amidyl Radicals by Oxidation of α-Amido-oxy Acids: Transition-Metal-Free Amidofluorination of Unactivated Alkenes,
H. Jiang, A. Studer,
Angew. Chem. Int. Ed. 2018, 57, 10707-10711. [doi:10.1002/anie.201804966];
among the top 10% most downloaded papers.
307.
Mixed AuPd‐Nanoparticles as Highly Active Catalysts for Alkyne Z‐Semihydrogenation,
M. Wissing, M. Niehues, B. J. Ravoo, A. Studer,
Eur. J. Org. Chem. 2018, 3403-3409. [doi:10.1002/ejoc.201800583];
highlighted in Synfacts 2018, 14(10), 1105.
306.
Transition Metal-Free 1,2-Carboboration of Unactivated Alkenes,
Y. Cheng, C. Mück-Lichtenfeld, A. Studer,
J. Am. Chem. Soc. 2018, 140, 6221-6225. [doi:10.1021/jacs.8b03333];
highlighted in Chem 2018, 4(6), 1205-1207;
highlighted in Synfacts 2018, 14(8), 0848.
305.
Short and Protecting-Group-Free Approach to the (‒)-Δ8-THC-Motif: Synthesis of THC-Analogues, (‒)-Machaeriol B and (‒)-Machaeriol D,
G. Hoffmann, A. Studer,
Org. Lett. 2018, 20, 2964-2966. [doi:10.1021/acs.orglett.8b01005];
correction: Org. Lett. 2019, 21, 340. [doi:10.1021/acs.orglett.8b03908]
304.
Optomechanically-assisted assembly of surface functionalized zeolite-L based hybrid soft matter,
A. Barroso, T. Buscher, K. Ahlers, A. Studer, C. Denz,
Part. Part. Syst. Char. 2018, 35, 180041-1-6. [doi:10.1002/ppsc.201800041]
303.
α-Diazo Ketones in On-Surface Chemistry,
L. Liu, H. Klaasen, A. Timmer, H.-Y. Gao, D. Barton, H. Mönig, J. Neugebauer, H. Fuchs, A. Studer,
J. Am. Chem. Soc. 2018, 140, 6000-6005. [doi:10.1021/jacs.8b02599];
showcased as Virtual Cover.
302.
Towards reliable references for electron paramagnetic resonance parameters based on quantum chemistry: the case of verdazyl radicals,
A. Massolle, T. Dresselhaus, S. Eusterwiemann, C. Doerenkamp, H. Eckert, A. Studer, J. Neugebauer,
Phys. Chem. Chem. Phys. 2018, 20, 7661-7675. [doi:10.1039/C7CP05657E]
301.
Lewis Acid Catalyzed Stereoselective Dearomative Coupling of Indolylboron Ate Complexes with D-A Cyclopropanes and Alkyl Halides,
S. Das, C. G. Daniliuc, A. Studer,
Angew. Chem. Int. Ed. 2018, 57, 4053-4057. [doi:10.1002/anie.201711923]
300.
Electrochemical Initiation of Electron-Catalyzed Phenanthridine Synthesis by Trifluoromethylation of Isonitriles,
M. Lübbesmeyer, D. Leifert, H. Schäfer, A. Studer,
Chem. Commun. 2018, 54, 2240-2243. [doi:10.1039/C7CC09302K]
299.
Visible-Light-Enabled Preparation of Palladium Nanoparticles and Application as Catalysts for Suzuki–Miyaura Coupling,
F. Mäsing, H. Nüsse, J. Klingauf, A. Studer,
Org. Lett. 2018, 20, 752-755. [doi:10.1021/acs.orglett.7b03892]
298.
Synthesis of α-Chiral Ketones and Chiral Alkanes Using Radical Polar Crossover Reactions of Vinyl Boron Ate Complexes,
C. Gerleve, M. Kischkewitz, A. Studer,
Angew. Chem. Int. Ed. 2018, 57, 2441-2444. [doi:10.1002/anie.201711390];
highlighted in Synfacts 2018, 14(04), 0415.
297.
α-Aminoxy Acid Auxiliary Enabled Intermolecular Radical γ-C(sp3)-H Functionalization of Ketones,
H. Jiang, A. Studer,
Angew. Chem. Int. Ed. 2018, 57, 1708-1712. [doi:10.1002/ange.201712066]
296.
Synthesis of Highly Substituted Arenes via Cyclohexadiene–Alkene C–H Cross Coupling and Aromatization,
A. Bhunia, A. Studer,
ACS Catal. 2018, 8, 1213-1217. [doi:10.1021/acscatal.8b00083]
295.
Alkene 1,2-difunctionalization via Radical Alkenyl Migration,
X. Tang, A. Studer,
Angew. Chem. Int. Ed. 2018, 57, 814-817. [doi:10.1002/anie.201710397]
 
294.
Molecular Recognition and Immobilization of Ligand Conjugated Redox-Responsive Polymer Nanocontainers,
W. de Vries, M. Tesch, A. Studer, B. J. Ravoo,
ACS Appl. Mater. Interfaces 2017, 9, 41760-41766. [doi:10.1021/acsami.7b15516]
293.
Reduction of Dioxygen by Radical/B(p-C6F4X)3 Pairs to Give Isolable Bis(borane)superoxide Compounds,
G. Erker, X. Tao, C. G. Daniliuc, O. Janka, R. Pöttgen, R. Knitsch, M. R. Hansen, H. Eckert, M. Lübbesmeyer, A. Studer, G. Kehr,
Angew. Chem. Int. Ed. 2017, 56, 16641-16644. [doi:10.1002/anie.201709309]
292.
1-Trifluoromethylisoquinolines from α-Benzylated Tosylmethyl Isocyanide Derivatives in a Modular Approach,
L. Wang, A. Studer,
Org. Lett. 2017, 19, 5701-5704. [doi:10.1021/acs.orglett.7b02882]
291.
Transition-Metal-Free Ring-Opening Silylation of Indoles and Benzofurans with (Diphenyl-tert-butylsilyl)lithium,
P. Xu, E.-U. Würthwein, C. G. Daniliuc,
Angew. Chem. Int. Ed. 2017, 56, 13872-13875. [doi:10.1002/anie.201707309]
290.
Radical Hydrodehalogenation of Aryl Bromides and Chlorides with Sodium Hydride and 1,4-Dioxane,
T. Hokamp, A. Dewanji, M. Lübbesmeyer, C. Mück-Lichtenfeld, E.-U. Würthwein, A. Studer,
Angew. Chem. Int. Ed. 2017, 56, 13275-13278. [doi:10.1002/anie.201706534]
289.
Iminyl-Radicals by Oxidation of α-Imino-oxy Acids: Photoredox-Neutral Alkene Carboimination for the Synthesis of Pyrrolines,
H. Jiang, A. Studer,
Angew. Chem. Int. Ed. 2017, 56, 12273-12276. [doi:10.1002/anie.201706270]
288.
Stereospecific 1,3-Aminobromination of Donor-Acceptor Cyclopropanes,
S. Das, C. G. Daniliuc, A. Studer,
Angew. Chem. Int. Ed. 2017, 56, 11554-11558. [doi:10.1002/anie.201704092]
287.
α-Perfluoroalkyl-β-alkynylation of alkenes via radical alkynyl migration,
X. Tang, A. Studer,
Chem. Sci. 2017, 8, 6888-6892. [doi:10.1039/C7SC02175E];
highlighted in Synfacts 2017, 13(11), 1186.
286.
Radical Difluoromethylation of Thiols with (Difluoromethyl)triphenylphosphonium Bromide,
N. B. Heine, A. Studer,
Org. Lett. 2017, 19, 4150-4153. [doi:10.1021/acs.orglett.7b02109]
285.
Iodine(III) Reagents in Radical Chemistry,
X. Wang, A. Studer,
Acc. Chem. Res. 2017, 50, 1712-1724. [doi:10.1021/acs.accounts.7b00148]
284.
Radical cascade cyclization of 1,n-enynes and diynes for the synthesis of carbocycles and heterocycles,
J. Xuan, A. Studer,
Chem. Soc. Rev. 2017, 46, 4329-4346. [doi:10.1039/C6CS00912C]
283.
Strong Intermolecular Antiferromagnetic Verdazyl-Verdazyl Coupling in the Solid State,
S. Eusterwiemann, C. Doerenkamp, T. Dresselhaus, O. Janka, M. de Oliveira, C. G. Daniliuc, H. Eckert, J. Neugebauer, R. Pöttgen, A. Studer,
Phys. Chem. Chem. Phys. 2017, 19, 15681-15685. [doi:10.1039/C7CP02950K]
282.
Perfluoroalkylation of Aryl-N,N-dimethyl Hydrazones Using Hypervalent Iodine (III) Reagents or Perfluoroalkyl Iodides,
B. Janhsen, A. Studer,
J. Org. Chem. 2017, 8211703-11710. [doi:10.1021/acs.joc.7b00934]
281.
Regio- and Stereoselective Radical Perfluoroalkyltriflation of Alkynes Using Phenyl(perfluoroalkyl)iodonium Triflates,
X. Wang, A. Studer,
Org. Lett. 2017, 19, 2977-2980. [doi:10.1021/acs.orglett.7b01215];
highlighted in Synfacts 2017, 13(8), 0830.
280.
Reversible Stabilization of Vesicles: Redox-Responsive Polymer Nanocontainers for Intracellular Delivery,
W. C. de Vries, D. Grill, M. Tesch, A. Ricker, H. Nüsse, J. Klingauf, A. Studer, V. Gerke, B. J. Ravoo,
Angew. Chem. Int. Ed. 2017, 56, 9603-9607. [doi:10.1002/anie.201702620];
showcased as Inside Front Cover.
279.
Light Mediated Preparation of Palladium Nanoparticles as Catalysts for Alkyne cis-Semihydrogenation,
F. Mäsing, H. Nüsse, J. Klingauf, A. Studer,
Org. Lett. 2017, 19, 2658-2661. [doi:10.1021/acs.orglett.7b00999];
highlighted in Synfacts 2017, 13(9), 0994.
278.
Oxidative N-Heterocyclic Carbene Catalyzed Dearomatization of Indoles to Spirocyclic Indolenines with Quaternary Carbon Stereocenter,
S. Bera, C. G. Daniliuc, A. Studer,
Angew. Chem. Int. Ed. 2017, 56, 7402-7406. [doi:10.1002/anie.201701485];
showcased as Front Cover;
highlighted in Synfacts 2017, 13(8), 0875.
277.
Intermolecular On-Surface σ-Bond Metathesis,
H.-Y. Gao, P. A. Held, S. Amirjalayer, L. Liu, A. Timmer, B. Schirmer, O. Díaz Arado, H. Mönig, C. Mück-Lichtenfeld, J. Neugebauer, A. Studer, H. Fuchs,
J. Am. Chem. Soc. 2017, 139, 7012-7019. [doi:10.1021/jacs.7b02430]
276.
Cooperative Magnetism in Crystalline N-Aryl-Substituted Verdazyl Radicals: First-Principles Predictions and Experimental Results,
S. Eusterwiemann, T. Dresselhaus, C. Doerenkamp, O. Janka, O. Niehaus, A. Masolle, C. G. Daniliuc, H. Eckert, R. Pöttgen, J. Neugebauer, A. Studer,
Chem. Eur. J. 2017, 23, 6069-6082. [doi:10.1002/chem.201700988]
275.
Stereoselective Palladium-Catalyzed Decarboxylative -Arylation of Acyclic ,-Unsaturated Carboxylic Acids,
I. Scheipers, E. Koch, A. Studer,
Org. Lett. 2017, 19, 1741-1743. [doi:10.1021/acs.orglett.7b00512]
274.
Initiating radical reactions with non-thermal plasma,
Y. Gorbanev, D. Leifert, A. Studer, S. O'Connell, V. Chechik,
Chem. Commun. 2017, 53, 3685-3688. [doi:10.1039/C7CC01157A]
273.
Radical-polar crossover reactions of vinylboron ate complexes,
M. Kischkewitz, K. Okamoto, C. Mück-Lichtenfeld, A. Studer,
Science 2017, 355, 936-938. [doi:10.1126/science.aal3803];
highlighted in the press;
highlighted in Nach. Chem. 2017, 65, 520;
highlighted in Synfacts2017, 13(06), 0593;
free access: click here...
272.
Cooperative Effects in Chemistry - Collaborative Research Center SFB 858 in Münster,
L. Tebben, A. Studer,
Chem. Eur. J. 2017, 23, 5857-5859. [doi:10.1002/chem.201700451];
showcased as Front Cover.
271.
Orthogonal Click Postfunctionalization of Alternating Copolymers Prepared by Nitroxide Mediated Polymerization,
M. Tesch, S. Kudruk, M. Letzel, A. Studer,
Chem. Eur. J. 2017, 23, 5915-5919. [doi:10.1002/chem.201605639]
270.
Formation of Organometallic Intermediate States in On-Surface Ullmann Couplings,
D. Barton, H.-Y. Gao, P. A. Held, A. Studer, H. Fuchs, N. L. Doltsinis, J. Neugebauer,
Chem. Eur. J. 2017, 23, 6190-6197. [doi:10.1002/chem.201605802]
269.
Intra- versus Intermolecular Electron Transfer in Radical Nucleophilic Aromatic Substitution of Dihalo(hetero)arenes – a Tool for Estimating π-Conjugation in Aromatic Systems,
B. Janhsen, C. G. Daniliuc, A. Studer,
Chem. Sci. 2017, 8, 3547-3553. [doi:10.1039/C7SC00100B]
268.
New AdoMet Analogues as Tools for Enzymatic Transfer of Photo-Cross-Linkers and Capturing RNA–Protein Interactions,
F. Muttach, F. Mäsing, A. Studer, A. Rentmeister,
Chem. Eur. J. 2017, 23, 5988-5993. [doi:10.1002/chem.201605663]
267.
Reaction of Arynes with Vinyl Sulfoxides: Highly Stereospecific Synthesis of ortho-Sulfinylaryl Vinyl Ethers,
Y. Li, A. Studer,
Org. Lett. 2017, 19, 666-669. [doi:10.1021/acs.orglett.6b03827]
266.
Covalent-bond formation via on-surface chemistry,
P. A. Held, H. Fuchs, A. Studer,
Chem. Eur. J. 2017, 23, 5874-5892. [doi:10.1002/chem.201604047]
265.
Synthesis and Physical Properties of Strained Doubly Phosphorus-Bridged Biaryls and Viologens,
T. W. Greulich, E. Yamaguchi, C. Doerenkamp, M. Lübbesmeyer, C. G. Daniliuc, A. Fukazawa, H. Eckert, S. Yamaguchi, A. Studer,
Chem. Eur. J. 2017, 23, 6029-6033. [doi:10.1002/chem.201605272]
264.
Palladium Nanoparticle Loaded Bifunctional Silica Hybrid Material: Preparation and Applications as Catalyst in Hydrogenation Reactions,
S. K. Surmiak, C. Doerenkamp, P. Selter, M. Peterlechner, A. H. Schäfer, H. Eckert, A. Studer,
Chem. Eur. J. 2017, 23, 6019-6028. [doi:10.1002/chem.201604508];
highlighted in Synfacts 2017, 13(8), 0993.
263.
Preparation of Functional Alternating Polymer Brushes and their Orthogonal Surface Modification via Microcontact Printing,
M. Buhl, M. Tesch, S. Lamping, J. Moratz, A. Studer, B. J. Ravoo,
Chem. Eur. J. 2017, 23, 6042-6047. [doi:10.1002/chem.201603565]
262.
Preparation of 4,6-Disubstituted α-Pyrones by Oxidative N-Heterocyclic Carbene Catalysis,
S. Bera, A. Studer,
Synthesis 2017, 49, 121-126. [doi:10.1055/s-0036-1588336]
261.
Facile Light-Mediated Preparation of Small Polymer-Coated Palladium -Nanoparticles and their Application as Catalysts for Alkyne Semi-Hydrogenation,
F. Mäsing, X. Wang, H. Nüsse, J. Klingauf, A. Studer,
Chem. Eur. J. 2017, 23, 6014-6018. [doi:10.1002/chem.201603297];
highlighted in Synfacts 2017, 13(8), 0881.
260.
From Additivity to Cooperativity in Chemistry - Can Cooperativity be Measured?,
L. Tebben, C. Mück-Lichtenfeld, G. Fernandez, S. Grimme, A. Studer,
Chem. Eur. J. 2017, 23, 5864-5873. [doi:10.1002/chem.201604651]
259.
The Chemistry of a Non-Interacting Vicinal Frustrated Phosphane/Borane Lewis Pair,
L.-M. Elmer, G. Kehr, C. G. Daniliuc, M. Siedow, H. Eckert, M. Tesch, A. Studer, K. Williams, T. H. Warren, G. Erker,
Chem. Eur. J. 2017, 23, 6056-6068. [doi:10.1002/chem.201603954]
 
258.
Construction of Polycyclic γ-Lactams and Related Heterocycles via Electron Catalysis,
J. Xuan, C. G. Daniliuc, A. Studer,
Org. Lett. 2016, 18, 6372-6375. [doi:10.1021/acs.orglett.6b03267]
257.
Multicomponent 1,3-Bifunctionalization of Donor-Acceptor Cyclopropanes with Arenes and Nitrosoarenes,
S. Das, C. G. Daniliuc, A. Studer,
Org. Lett. 2016, 18, 5576-5579. [doi:10.1021/acs.orglett.6b02815]
256.
Sulfonium Ylides via (3+2) Cycloaddition of Arynes with Vinyl Sulfides - Stereoselective Synthesis of Highly Substituted Alkenes,
Y. Li, C. Mück-Lichtenfeld, A. Studer,
Angew. Chem. Int. Ed. 2016, 55, 14435-14438. [doi:10.1002/anie.201608144]
255.
Black-Box Determination of Temperature-dependent Susceptibilities for Crystalline Organic Radicals with Complex Magnetic Topologies,
T. Dresselhaus, S. Eusterwiemann, D. R. Matuschek, C. G. Daniliuc, O. Janka, R. Pöttgen, A. Studer, J. Neugebauer,
Phys. Chem. Chem. Phys. 2016, 18, 28262-28273. [doi:10.1039/C6CP05875B]
254.
Understanding molecular self-assembly of a diol compound by considering competitive interactions,
O. Díaz Arado, M. Luft, H. Mönig, P.-A. Held, A. Studer, S. Amirjalayer, H. Fuchs,
Phys. Chem. Chem. Phys. 2016, 18, 27390-27395. [doi:10.1039/C6CP05818C]
253.
Radical Cascade Cyclization - Reaction of 1,6-Enynes with Aryl Radicals via Electron-Catalysis,
J. Xuan, D. Gonzalez-Abradelo, C. A. Strassert, C.-G. Daniliuc, A. Studer,
Eur. J. Org. Chem. 2016, 4961-4964. [doi:10.1002/ejoc.201601033]
252.
Sodium-Ketyl Radical Anions by Reverse Pinacol Reaction and their Coupling with Iodoarenes,
X. Tang, A. Studer,
Org. Lett. 2016, 18, 4448-4450. [doi:10.1021/acs.orglett.6b02184]
251.
Iodinated (Perfluoro)alkyl Quinoxalines via Atom Transfer Radical Addition using ortho-Diisocyanoarenes as Radical Acceptors,
D. Leifert, A. Studer,
Angew. Chem. Int. Ed. 2016, 55, 11660-11663. [doi:10.1002/anie.201606023]
250.
Electron-Catalyzed Fluoroalkylation of Vinyl Azides,
E. G. Mackay, A. Studer,
Chem. Eur. J. 2016, 22, 13455-13458. [doi:10.1002/chem.201602855]
249.
On-Surface Domino Reactions: Glaser Coupling and Dehydrogenative Coupling of a Biscarboxylic Acid to Form Polymeric Bisacylperoxides,
P. A. Held, H.-Y. Gao, L. Liu, C. Mück-Lichtenfeld, A. Timmer, H. Mönig, D. Barton, J. Neugebauer, H. Fuchs, A. Studer,
Angew. Chem. Int. Ed. 2016, 55, 9777-9782. [doi:10.1002/anie.201602859]
248.
Poly(paraphenylene sulfide) and Poly(metaphenylene sulfide) via Light-initiated SRN1-type Polymerization of Halogenated Thiophenols,
N. B. Heine, A. Studer,
Macrom. Rapid Commun. 2016, 37, 1494-1498. [doi:10.1002/marc.201600254];
showcased as Front Cover.
247.
Tetrahydroquinolines via Stereospecific [3+3]-Annulation of 2 Donor−Acceptor Cyclopropanes with Nitrosoarenes,
S. Das, S. Chakrabarty, C. G. Daniliuc, A. Studer,
Org. Lett. 2016, 18, 2784-2787. [doi:10.1021/acs.orglett.6b01302]
246.
Synthesis of chiral piperazinones using amphoteric aziridine aldehyde dimers and functionalized isocyanides,
N. B. Heine, S. J. Kaldas, L. Belding, O. Shmatova, T. Dudding, V. G. Nenajdenko, A. Studer, A. K. Yudin,
J. Org. Chem. 2016, 81, 5209-5216. [doi:10.1021/acs.joc.6b00471];
highlighted in Synfacts 2016, 12(8), 0786.
245.
Radical Hydrodeiodination of Aryl, Alkenyl, Alkynyl and Alkyl Iodides with an Alcoholate as Organic Chain Reductant via Electron-Catalysis,
A. Dewanji, C. Mück-Lichtenfeld, A. Studer,
Angew. Chem. Int. Ed. 2016, 55, 6749-6752 . [doi:10.1002/anie.201601930]
244.
Exploring Cooperative Effects in Oxidative NHC Catalysis – Regioselective Acylation of Carbohydrates,
D. L. Cramer, S. Bera, A. Studer,
Chem. Eur. J. 2016, 22, 7403-7407. [doi:10.1002/chem.201601398]
243.
Palladium-Catalyzed Dearomatizing Difunctionalization of Indoles and Benzofurans,
V. Ramella, Z. He, C. Daniliuc, A. Studer,
Eur. J. Org. Chem. 2016, 2268-2273. [doi:10.1002/ejoc.201600194]
242.
Synthesis of a Bulky Nitroxide and Its Application in the Nitroxide-mediated Radical Polymerization,
Y. Jing, M. Tesch, L. Wang, C. G. Daniliuc, A. Studer,
Tetrahedron 2016, 72, 7665-7671. [doi:10.1016/j.tet.2016.04.008]
241.
Radical Perfluoroalkylation – Easy Access to 2 Perfluoroalkylindol-3-imines via Electron Catalysis,
D. Leifert, D. G. Artiukhin, J. Neugebauer, A. Galstyan, C. A. Strassert, A. Studer,
Chem. Commun. 2016, 52, 5997-6000. [doi:10.1039/C6CC02284G]
240.
Effect of the C3-Substituent in Verdazyl Radicals on their Profluorescent Behaviour,
S. Eusterwiemann, D. Matuschek, L. Stegemann, S. Klabunde, C. Doerenkamp, C. G. Daniliuc, N. L. Doltsinis, C. A. Strassert, H. Eckert, A. Studer,
Chimia 2016, 70(3), 172-176. [doi:10.2533/chimia.2016.172]
239.
3-Alkylperoxy-3-cyano-oxindoles from 2-Cyano-2-diazo-N-phenyl-acetamides via Cyclizing Carbene-Insertion and Subsequent Radical Oxidation,
M. Kischkewitz, C.-G. Daniliuc, A. Studer,
Org. Lett. 2016, 18, 1206-1209. [doi:10.1021/acs.orglett.6b00367]
238.
Regio- and Stereoselective Cyanotriflation of Alkynes Using Aryl(cyano)iodonium Triflates,
X. Wang, A. Studer,
J. Am. Chem. Soc. 2016, 138, 2977-2980. [doi:10.1021/jacs.6b00869];
highlighted in C&EN 2016, 94(9), 12,
highlighted in Nach. Chem. 2015, 64, 495.
237.
Generation of Aryl Radicals via Reduction of Hypervalent Iodine (III) Compounds with TEMPONa - Radical Alkene Oxyarylation,
M. Hartmann, Y. Li, C. Mück-Lichtenfeld. A. Studer,
Chem. Eur. J. 2016, 22, 3485-3490. [doi:10.1002/chem.201504852]
236.
Synthesis and Characterization of amorphous mesoporous silica using TEMPO-functionalized amphiphilic templates,
W. de Vries, C. Doerenkamp, Z. Zeng, M. de Oliveira Junior, O. Niehaus, R. Pöttgen, A. Studer, H. Eckert,
J. Sol. State Chem. 2016, 237, 93-98. [doi:10.1016/j.jssc.2016.01.023]
235.
FLPNO Nitroxide Radical Formation by a 1,1-Carboboration Route,
R. Liedtke, C. Eller, C. G. Daniliuc, K. Williams, T. H. Warren, M. Tesch, A. Studer, G. Kehr, G. Erker,
Organometallics 2016, 35, 55-61. [doi:10.1021/acs.organomet.5b00886]
234.
A biphenyl containing two electron-donating and two accepting moieties: a rigid and small donor-acceptor-donor ladder system,
T. W. Greulich, N. Suzuki, C. G. Daniliuc, A. Fukazawa, E. Yamaguchi, A. Studer, S. Yamaguchi,
Chem. Commun. 2016, 52, 2374-2377. [doi:10.1039/C5CC03063C];
highlighted in Synfacts 2016, 12(3), 0249.
233.
Selective N,O-Addition of the TEMPO Radical to Conjugated Boryl Dienes,
F. Türkyilmaz, G. Kehr, C. G. Daniliuc, M. Tesch, A. Studer, G. Erker,
Angew. Chem. Int. Ed. 2016, 55, 1470-1473. [doi:10.1002/anie.201509114]
232.
Ortho-Trialkylstannyl Arylphosphanes by C-P and C-Sn Bond Formation in Arynes,
Y. Li, S. Chakrabarty, C. Mück-Lichtenfeld, A. Studer,
Angew. Chem. Int. Ed. 2016, 55, 802-806. [doi:10.1002/anie.201509329]
231.
Determination of Rate Constants for Trifluoromethyl Radical Addition to Various Alkenes via a Practical Method,
M. Hartmann, Y. Li, A. Studer,
Org. Biomol. Chem. 2016, 14, 206-210. [doi:10.1039/C5OB02210J]
230.
Intramolecular Radical Carboaminoxylation of Aryl Amines,
M. Hartmann, C. Gerleve, A. Studer,
Synlett 2016, 27, 724-730. [doi:10.1055/s-0035-1560770]
229.
Catalysis of Radical Reactions: A Radical Chemistry Perspective,
A. Studer, D. P. Curran,
Angew. Chem. Int. Ed. 2016, 55, 58-102. [doi:10.1002/anie.201505090]
 
228.
Enantioselective Synthesis of Substituted δ-Lactones by Cooperative Oxidative N-Heterocyclic Carbene and Lewis Acid Catalysis,
S. Bera, C. G. Daniliuc, A. Studer,
Org. Lett. 2015, 17, 4940-4943. [doi:10.1021/acs.orglett.5b01932]
227.
Controlled Light Mediated Preparation of Gold Nanoparticles via Norrish Type I Reaction of Photoactive Polymers,
F. Mäsing, A. Mardyukov, C. Doerenkamp, H. Eckert, U. Malkus, H. Nüsse, J. Klingauf, A. Studer,
Angew. Chem. Int. Ed. 2015, 54, 12612-12617. [doi:10.1002/anie.201505133]
226.
C-F Activation in Perfluorinated Arenes with Isonitriles under UV-Light Irradiation,
A. Dewanji, C. Mück-Lichtenfeld, K. Bergander, C. G. Daniliuc, A. Studer,
Chem. Eur. J. 2015, 21, 12295-12298. [doi:10.1002/chem.201502298]
225.
2,2'-Bis-substituted Biphenyls via Addition of Nucleophiles to Benzyne, Followed by in situ Oxidative Homocoupling,
F. Sibbel, C. G. Daniliuc, A. Studer,
Eur. J. Org. Chem. 2015, 4635-4644. [doi:10.1002/ejoc.201500456]
224.
Short and Divergent Total Synthesis of (+)-Macheriol B, (+)-Macheriol D, (+)-Δ8-THC, and Analogoues,
F. Klotter, A. Studer,
Angew. Chem. Int. Ed. 2015, 54, 8547-8550. [doi:10.1002/anie.201502595];
showcased as Inside Back Cover.
223.
Profluorescent verdazyl radicals - synthesis and characterization,
D. Matuschek, S. Eusterwiemann, C. Doerenkamp, L. Stegemann, C. A. Strassert, B. Wibbeling, C. G. Daniliuc, N. L. Doltsinis, H. Eckert, A. Studer,
Chem. Sci. 2015, 6, 4712-4716. [doi:10.1039/C5SC00724K]
222.
Stereoselective formation of coordination polymers with 1,4-diaminonaphthalene on variuous Cu substrates,
M. Knor, H.-Y. Gao, S. Amirjalayer, A. Studer, H. Gao, S. Du, H. Fuchs,
Chem. Commun. 2015, 51, 10854-10857. [doi:10.1039/C5CC03130C]
221.
Synthesis and Photo-Postmodification of Zeolite L Based Polymer Brushes,
T. Buscher, A. Barroso, C. Denz, A. Studer,
Polym. Chem. 2015, 6, 4221-4229. [doi:10.1039/C5PY00425J]
220.
Recent advances in the synthesis of nitrogen heterocycles via radical cascade reactions using isonitriles as radical acceptors,
B. Zhang, A. Studer,
Chem. Soc. Rev. 2015, 44, 3505-3521. [doi:10.1039/c5cs00083a]
219.
Nanoassembled dynamic optical waveguides and sensors based on zeolite L nanocontainers,
A. Barroso, K. Dieckmann, C. Alpmann, T. Buscher, A. Studer, C. Denz,
Proc. SPIE 9379, Complex Light and Optical Forces IX, 93790U, 2015, [doi:10.1117/12.2079156]
218.
Alternating Copolymerization by Nitroxide-Mediated Polymerization and Subsequent Orthogonal Functionalization,
M. Tesch, J. A. M. Hepperle, H. Klaasen, M. Letzel, A. Studer,
Angew. Chem. Int. Ed. 2015, 54, 5054-5059. [doi:10.1002/anie.201412206];
highlighted in Nach. Chem. 2015, 63, 619.
217.
In-plane Van der Waals Interactions of Molecular Self-assembly Monolayer,
H. Y. Gao, H. Wagner, P. A. Held, S. Du, H.-J. Gao, A. Studer, H. Fuchs,
Appl. Phys. Lett. 2015, 106, 081606-1-5. [doi:10.1063/1.4907777]
216.
Radical Aminooxygenation of Alkenes with N-fluoro-benzenesulfonimide (NFSI) and TEMPONa,
Y. Li, M. Hartmann, C. G. Daniliuc, A. Studer,
Chem. Commun. 2015, 51, 5706-5709. [doi:10.1039/C5CC00591D]
215.
On-Surface Reductive Coupling of Aldehydes on Au(111),
O. D. Arado, H. Mönig, J.-H. Franke, A. Timmer, P. A. Held, A. Studer, H. Fuchs,
Chem. Commun. 2015, 51, 4887-4890. [doi:10.1039/C4CC09634G]
214.
Optical assembly of bio-hybrid micro-robots,
A. Barrosso, S. Landwerth, M. Woerdemann, C. Alpmann, T. Buscher, M. Becker, A. Studer, C. Denz,
Biomed Microdevices 2015, 17, 26-1-8. [doi:10.1007/s10544-015-9933-1]
213.
An Efficient Approach to Chiral Allyloxyamines via Stereospecific Allylation of Nitrosoarenes with Chiral Allylboronates,
Y. Li, S. Chakrabarty, A. Studer,
Angew. Chem. Int. Ed. 2015, 54, 3587-3591. [doi:10.1002/anie.201410188]
212.
Palladium-Catalyzed Diastereoselective Oxyarylation of 2-Alkylindoles,
V. Ramella, Z. He, C. Daniliuc, A. Studer,
Org. Lett. 2015, 17, 664-667. [doi:10.1021/ol503689r];
highlighted in Synfacts 2015, 11, 395.
211.
Fabrication of Hydrophilic Polymer Nanocontainers using Supramolecular Templates,
A. Samanta, M. Tesch, U. Keller, J. Klingauf, A. Studer, B. J. Ravoo,
J. Am. Chem. Soc. 2015, 137, 1967-1971. [doi:10.1021/ja511963g]
210.
Preparation of phenanthrenes from ortho-amino-biphenyls and alkynes via base-promoted homolytic aromatic substitution,
M. Hartmann, C. G. Daniliuc, A. Studer,
Chem. Commun. 2015, 51, 3121-3123. [doi:10.1039/C4CC10063H];
highlighted in Synfacts 2015, 11, 381.
209.
TEMPO-Mediated Homocoupling of Aryl Grignard Reagents: Mechanistic Studies,
S. Murarka, J. Möbus, G. Erker, C. Mück-Lichtenfeld, A. Studer,
Org. Biomol. Chem. 2015, 13, 2762-2767. [doi:10.1039/C4OB02689F]
208.
N-Aminopyridinium Salts as Precursors for N-Centered Radicals - Direct Amidation of Arenes and Heteroarenes,
T. W. Greulich, C. G. Daniliuc, A. Studer,
Org. Lett. 2015, 17, 254-257. [doi:10.1021/ol503338b];
selected as Editor's Choice article.
207.
9-Silafluorenes via Base-promoted Homolytic Aromatic Substitution (BHAS) – The Electron as a Catalyst,
D. Leifert, A. Studer,
Org. Lett. 2015, 17, 386-389. [doi:10.1021/ol503574k]
206.
Ni-Catalyzed α-arylation of esters and amides with phenol derivatives,
E. Koch, R. Takise, A. Studer, J. Yamaguchi, K. Itami,
Chem. Commun. 2015, 51, 855-857. [doi:10.1039/C4CC08426H]
205.
Stereoselective Lewis Base Catalyzed Formal 1,3-Dipolar Cycloaddition of Azomethine Imines with Mixed Anhydrides,
L. Hesping, A. Biswas, C. G. Daniliuc, C. Mück-Lichtenfeld, A. Studer,
Chem. Sci. 2015, 6, 1252-1257. [doi:10.1039/C4SC02612H]
 
204.
1-Trifluoromethylated isoquinolines via radical trifluoromethylation of isonitriles,
B. Zhang, A. Studer,
Org. Biomol. Chem. 2014, 12, 9895-9898. [doi:10.1039/C4OB02145B ]
203.
Direct Conversion of Alcohols to α-Chloro Aldehydes and α-Chloro Ketones,
Y. Jing, C. G. Daniliuc, A. Studer,
Org. Lett. 2014, 16, 4932-4935. [doi:10.1021/ol5024568]
202.
The Electron is a Catalyst,
A. Studer, D. P. Curran,
Nat. Chem. 2014, 6, 765-773. [doi:10.1038/nchem.2031]
201.
Surface Patterning with Natural and Synthetic Polymers via an Inverse Electron Demand Diels-Alder Reaction Employing Microcontact Chemistry,
O. Roling, A. Mardyukov, S. Lamping, B. Vonhören, S. Rinnen, H. F. Arlinghaus, A. Studer, B. J. Ravoo,
Org. Biomol. Chem. 2014, 12, 7828-7835. [doi:10.1039/C4OB01379D]
200.
6-Perfluoroalkylated Phenanthridines via Radical Perfluoroalkylation of Isonitriles,
B. Zhang, A. Studer,
Org. Lett. 2014, 16, 3990-3993. [doi:10.1021/ol5018195]
199.
N-heterocyclic carbene catalysed oxidative esterification of aliphatic aldehydes,
R. C. Samantha, A. Studer,
Org. Chem. Front. 2014, 1(8), 936-939. [doi:10.1039/C4QO00164H]
198.
Asymmetric Synthesis of Highly Substituted β-Lactones via Oxidative Carbene Catalysis with LiCl as Cooperative Lewis Acid,
S. Bera, R. C. Samanta, C. G. Daniliuc, A. Studer,
Angew. Chem. Int. Ed. 2014, 53, 9622-9626. [doi:10.1002/anie.201405200];
highlighted in Synfacts 2014 10(10), 1089.
197.
Cyclizing Radical Carboiodination, Carbotelluration and Carboaminoxylation of Aryl Amines,
M. Hartmann, A. Studer,
Angew. Chem. Int. Ed. 2014, 53, 8180-8183. [doi:10.1002/anie.201403968]
196.
Decarboxylative Polymerization of 2,6-Naphthalenedicarboxylic Acid at Surfaces,
H.‐Y. Gao, P. A. Held, M. Knor, C. Mück‐Lichtenfeld, J. Neugebauer, A. Studer, H. Fuchs,
J. Am. Chem. Soc. 2014, 136, 9658-9663. [doi:10.1021/ja5033875]
195.
Synthesis of Bulky Nitroxides, Characterization, and Their Application in Controlled Radical Polymerization,
Y. Jing, A. Mardyukov, K. Bergander, C. G. Daniliuc, A. Studer,
Macromolecules 2014, 47, 3595–3602. [doi:10.1021/ma500639y]
194.
Stereospecific Formal [3+2] Dipolar Cycloaddition of Cyclopropanes with Nitrosoarenes - An Approach to Isoxazolidines,
S. Chakrabarty, I. Chatterjee, B. Wibbeling, C. G. Daniliuc, A. Studer,
Angew. Chem. Int. Ed. 2014, 53, 5964–5968. [doi:10.1002/anie.201400885]
193.
Polymer Brushes Exhibiting Versatile Supramolecular Interactions Grown by Nitroxide-Mediated Polymerization and Structured via Microcontact Chemistry,
O. Roling, A. Mardyukov, J. A. Krings, A. Studer, B. J. Ravoo,
Macromolecules 2014, 47, 2411–2419. [doi:10.1021/ma500043b]
192.
Photochemical Glaser Coupling at Metal Surfaces,
H.-Y. Gao, D. Zhong, H. Mönig, H. Wagner, P.-A. Held, A. Timmer, A. Studer, H. Fuchs,
J. Phys. Chem. C 2014, 118,6272–6277. [doi:10.1021/jp411889e]
191.
Copper-Catalyzed Intermolecular Aminoazidation of Alkenes,
B. Zhang, A. Studer,
Org. Lett. 2014, 16, 1790–1793. [doi:10.1021/ol500513b];
highlighted in Synfacts 2014 10(5), 0485.
190.
Total Synthesis of Resveratrol-Based Natural Products Using a Palladium-Catalyzed Decarboxylative Arylation and an Oxidative Heck Reaction,
F. Klotter, A. Studer,
Angew. Chem. Int. Ed. 2014, 53, 2473-2476. [doi:10.1002/anie.201310676];
showcased as Front Cover,
selected as Hot Paper,
highlighted in Synfacts 2014 10(5), 0447 and
highlighted in Nach. Chem. 2014, 62, 403.
189.
2-Trifluoromethylated Indoles via Radical Trifluoromethylation of Isonitriles,
B. Zhang, A. Studer,
Org. Lett. 2014, 16, 1216-1219. [doi:10.1021/ol5001395]
188.
UV-Vis-monitoring of radical polymerization by spin trapping with chromophoric nitrones,
R. Husmann, S. Wertz, C. G. Daniliuc, S. W. Schäfer, C. B. McArdle, A. Studer,
Macromolecules 2014, 47, 993-1000. [doi:10.1021/ma4025174]
187.
6-Phosphorylated Phenanthridines from 2-Isocyanobiphenyls via Radical C-P and C-C Bond Formation ,
B. Zhang, C. G. Daniliuc, A. Studer,
Org. Lett. 2014, 16, 250-253. [doi:10.1021/ol403256e]
186.
Selective Synthesis of [7]- and [8]Cycloparaphenylenes,
F. Sibbel, K. Matsui, Y. Segawa, A. Studer, K. Itami,
Chem. Commun. 2014, 50, 954-956. [doi:10.1039/C3CC48683D]
185.
Synthesis of Orthogonally Addressable Block Copolymers via Reversible Addition Fragmentation Chain Transfer (RAFT) Polymerization and Subsequent Chemoselective Postmodification,
A. Mardyukov, M. Tesch, A. Studer,
J. Polym. Sci. Part A: Polym. Chem. 2014, 52, 258-266. [doi:10.1002/pola.26998]
184.
Synthesis of Dihydrobenzo[b]furans by Diastereoselective Acyloxyarylation,
K. Hata, Z. He, C. G. Daniliuc, K. Itami, A. Studer,
Chem. Commun. 2014, 50, 463-465. [doi:10.1039/C3CC47350C ]
 
183.
Oxidative Heck Coupling of Allylic Amines with 2,2,6,6-Tetramethylpiperidine-N-oxyl (TEMPO) as an Oxidant for Preparation of Tetrasubstituted Alkenes,
Z. He, B. Wibbeling, A. Studer,
Adv. Synth. Catal. 2013, 355, 3639-3647. [doi:10.1002/adsc.201300846]
182.
The renaissance of organic radical chemistry – deja vu all over again,
C. R. J. Stephenson, A. Studer, D. P. Curran,
Beilstein J. Org. Chem. 2013, 9, 2778-2780. [doi:10.3762/bjoc.9.312]
181.
6-Aroylated Phenanthridines via Base Promoted Homolytic Aromatic Substitution (BHAS),
D. Leifert, C. G. Daniliuc, A. Studer,
Org. Lett. 2013, 15, 6286-6289. [doi:10.1021/ol403147v]
180.
Phenyl Hydrazine as Initiator for Direct Arene C-H Arylation via Base Promoted Homolytic Aromatic Substitution,
A. Dewanji, S. Murarka, D. Curran, A. Studer,
Org. Lett. 2013, 15, 6102-6105. [doi:10.1021/ol402995e]
179.
Transition Metal-Functionalized PAMAM Dendrimers Encapsulated in PPX Tubes as Reusable Catalysts,
F. Mitschang, B. Dettlaff, J.-P. Lindner, A. Studer, A. Greiner,
Macromolecules 2013, 46,8784-8789. [doi:10.1021/ma401815x]
178.
Immobilization of Catalysts into Poly(p-xylylene) Nanotubes,
J. A. M. Hepperle, F. Mitschang, A. K. Bier, B. K. Dettlaff, A. Greiner, A. Studer,
RSC Adv. 2013, 3, 25976-25981. [doi:10.1039/C3RA43647K]
177.
On-Surface Azide–Alkyne Cycloaddition on Au(111),
O. Díaz Arado, H. Mönig, H. Wagner, J.-H. Franke, G. Langewisch, P. A. Held, A. Studer, H. Fuchs,
ACS Nano 2013, 7, 8509-8515. [doi:10.1021/nn4022789]
176.
6-Trifluorometyl-Phenanthridines through Radical Trifluoromethylation of Isonitriles,
B. Zhang, C. Mück-Lichtenfeld, C. G. Daniliuc, A. Studer,
Angew. Chem. Int. Ed. 2013, 52, 10792-10795. [doi:10.1002/anie.201306082];
selected as Hot Paper, highlighted in Synfacts, 2014, 10, 16.
175.
Nitroxide-Catalyzed Transition-Metal-Free Aerobic Oxidation Processes,
S. Wertz, A. Studer,
Green Chem. 2013, 15, 3116-3134. [doi:10.1039/C3GC41459K ]
174.
The Effect of Metal Surfaces in On-Surface Glaser-Coupling,
H.-Y. Gao, J.-H. Franke, H. Wagner, D. Zhong, P.-A. Held, A. Studer, H. Fuchs,
J. Phys. Chem. C 2013, 117, 18595–18602. [doi:10.1021/jp406858p]
173.
Stereoselective Radical Azidooxygenation of Alkenes,
B. Zhang, A. Studer,
Org. Lett. 2013, 15, 4548–4551. [doi:10.1021/ol402106x]
172.
Pd Immobilized in Mesoporous Silica Particles as Recyclable Catalysts for Suzuki-Miyaura Coupling: Cooperative Effects Exerted by Co-Immobilized Amine Functionalities,
A. T. Dickschat, S. Surmiak, A. Studer,
Synlett 2013, 24, 1523-1528. [doi:10.1055/s-0033-1339183]
171.
N-Heterocyclic Carbene Catalyzed Transesterification of poly-Trifluoroethyl-Acrylates,
J. A. M. Hepperle, R. C. Samanta, A. Studer,
Synlett 2013, 24, 1233-1237. [doi:10.1055/s-0033-1338950]
170.
Chemical Modification of Polymer Brushes via Nitroxide Photoclick Trapping,
A. Mardyukov, Y. Li, A. Dickschat, A. H. Schäfer, A. Studer,
Langmuir 2013, 29, 6369–6376. [doi:10.1021/la401179s]
169.
Synthesis and characterization of inorganic-organic hybrid materials based on the intercalation of stable organic radicals into fluoromica clay,
Z. Zeng, D. Matuschek, A. Studer, C. Schwickert, R. Pöttgen, H. Eckert
Dalton Trans. 2013, 42, 8585-8596. [doi:10.1039/C3DT50627D ]
168.
Cooperative N-heterocyclic carbene (NHC) and ruthenium redox catalysis: oxidative esterification of aldehydes with air as the terminal oxidant,
J. Zhao, C. Mück-Lichtenfeld, A. Studer,
Adv. Synth. Catal. 2013, 355, 1098-1106. [doi:10.1002/adsc.201300034]
167.
Assembly of linear chains consisting of alternating silica beads and zeolite L crystals by nitroxide exchange reaction,
M. Becker, L. De Cola, A. Studer,
J. Mater. Chem. C 2013, 1, 3287-3290. [doi:10.1039/C3TC30358F ];
showcased as Front Cover.
166.
Regioselective Threefold Aromatic Substitution of Benzoic Acid Derivatives via Dearomatization, Regioselective Functionalization and Rearomatization,
E. Koch, A. Studer,
Angew. Chem. Int. Ed. 2013, 52, 4933-4936. [doi:10.1002/anie.201300259];
highlighted in Nach. Chem. 2013, 61, 742.
165.
Polynitroxides from Alkoxyamine Monomers: Structural and Kinetic Investigations by Solid State NMR,
F. Behrends, H. Wagner, A. Studer, O. Niehaus, R. Pöttgen, H. Eckert,
Macromolecules 2013, 46, 2553-2561. [doi:10.1021/ma400351q]
164.
N-Heterocyclic Carbene (NHC) Catalyzed Chemoselective Acylation of Alcohols in the Presence of Amines with Various Acylating Reagents,
R. C. Samantha, S. De Sarkar, R. Fröhlich, S. Grimme, A. Studer,
Chem. Sci. 2013, 4, 2177-2184. [doi:10.1039/C3SC00099K]
163.
Catalysis with N-Heterocyclic Carbenes under Oxidative Conditions,
S. De Sarkar, A. Biswas, R. C. Samanta, A. Studer,
Chem. Eur. J. 2013, 19, 4664-4678. [doi:10.1002/chem.201203707]
162.
Glaser Coupling at Metal Surfaces,
H.-Y. Gao, H. Wagner, D. Zhong, J.-H. Franke, A. Studer, H. Fuchs,
Angew. Chem. Int. Ed. 2013, 52, 4024-4028. [doi:10.1002/anie.201208597];
showcased as Front Cover.
161.
Cross Dehydrogenative Coupling via Base-promoted Homolytic Aromatic Substitution (BHAS) - Synthesis of Fluorenones and Xanthones,
S. Wertz, D. Leifert, A. Studer,
Org. Lett. 2013, 15, 928-931. [doi:10.1021/ol4000857]
160.
Reactions of Arynes with Nitrosoarenes-An Approach to Substituted Carbazoles,
S. Chakrabarty, I. Chatterjee, L. Tebben, A. Studer,
Angew. Chem. Int. Ed. 2013, 52, 2968-2971. [doi:10.1002/anie.201209447];
highlighted in Synfacts 2013 9(7), 0705 and Synfacts 2013, 9(5), 0539.
159.
Bifunctional mesoporous silica nanoparticles as cooperative catalysts for the Tsuji–Trost reaction – tuning the reactivity of silica nanoparticles,
A. T. Dickschat, F. Behrends, S. Surmiak, M. Weiß, H. Eckert, A. Studer,
Chem. Commun. 2013, 49, 2195-2197. [doi:10.1039/C3CC00235G]
158.
AFM-Based Force Spectroscopy on Polystyrene Brushes: Effect of Brush Thickness on Protein Adsorption,
C. Hentschel, H. Wagner, J. Smiatek, A. Heuer, H. Fuchs, X. Zhang, A. Studer, L. Chi,
Langmuir 2013, 29, 1850-1856. [doi:10.1021/la302212h]
157.
Preparation of Photoactive Polymers and Postmodification via Nitroxide Trapping under UV Irradiation,
A. Mardyukov, A. Studer,
Macromol. Rapid. Commun. 2013, 34, 94-101. [doi:10.1002/marc.201200595]
 
156.
Preparation of Bifunctional Mesoporous Silica Nanoparticles by Orthogonal Click Reactions and their Application in Cooperative Catalysis,
A. T. Dickschat, F. Behrends, M. Bühner, J. Ren, M. Weiß, H. Eckert, A. Studer,
Chem. Eur. J. 2012, 18, 16689-16697. [doi:10.1002/chem.201200499]
155.
Radical/Anionic SRN1-Type Polymerization for Preparation of Oligoarenes,
S. Murarka, A. Studer,
Angew. Chem. Int. Ed. 2012, 51, 12362-12366. [doi:10.1002/anie.201206096];
highlighted in Synfacts 2013, 9(2), 0154; reported in C&EN.
154.
Metal-Free 2,2,6,6-Tetramethylpiperidine-N-oxyl Radical (TEMPO) Catalyzed Aerobic Oxidation of Hydroxyl- and Alkoxyamines to Oximes and Oxime Ethers,
S. Wertz, A. Studer,
Helv. Chim. Acta 2012, 95, 1758-1772. [doi:10.1002/hlca.201200175]
153.
Transition-Metal-Free Oxyarylation of Alkenes with Aryl Diazonium Salts and TEMPONa,
M. Hartmann, Y. Li, A. Studer,
J. Am. Chem. Soc. 2012, 134, 16516-16519. [doi:10.1021/ja307638u]
152.
α-Aminoxylation of Ketones and β-Chloro-α-aminoxylation of Enones with TEMPO and Chlorocatecholborane,
Y. Li, M. Pouliot, T. Vogler, P. Renaud, A. Studer,
Org. Lett. 2012, 14, 4474-4477. [doi:10.1021/ol301979b]
151.
A "Renaissance" in Radical Trifluormethylation,
A. Studer,
Angew. Chem. Int. Ed. 2012, 51, 8950-8958. [doi:10.1002/anie.201202624]
150.
Transition-Metal-Free Trifluoromethylaminoxylation of Alkenes,
Y. Li, A. Studer,
Angew. Chem. Int. Ed. 2012, 51, 8221-8224. [doi:10.1002/anie.201202623];
selected as Hot Paper.
149.
Transition-Metal-Free Oxidative Coupling Reactions for the Formation of C-C and C-N Bonds by TEMPO and its Derivatives,
S. Murarka, S. Wertz, A. Studer,
Chimia 2012, 66, 413-417. [doi:10.2533/chimia.2012.413]
148.
N,N-Addition of Frustrated Lewis Pairs to Nitric Oxide: An Easy Entry to a Unique Family of Aminoxyl Radicals,
M. Sajid, A. Stute, A. Cardenas, B. Culotta, J. A. M. Hepperle, T. Warren, B. Schirmer, S. Grimme, A. Studer, C. Daniliuc, R. Fröhlich, G. Kehr, G. Erker,
J. Am. Chem. Soc. 2012, 134, 10156-10168. [doi:10.1021/ja302652a];
reported in C&EN 2012, 90(21), 7.
147.
Nucleophilic Addition of Enols and Enamines to α,β-Unsaturated Acyl Azoliums: Mechanistic Studies,
R. C. Samantha, B. Maji, S. De Sarkar, K. Bergander, R. Fröhlich, C. Mück-Lichtenfeld, H. Mayr, A. Studer,
Angew. Chem. Int. Ed. 2012, 51, 5234-5238. [doi:10.1002/anie.201109042]
146.
Nitroxide Mediated Polymerization of Styrene, n-Butyl Acrylate and Methyl Metacrylate Using Microflow Reactor Technology,
T. Fukuyama, Y. Kajihara, I. Ryu, A. Studer,
Synthesis 2012, 44, 2555-2559. [doi:10.1055/s-0031-1290780]
145.
Enantioselective Cyclopropanation of Enals by Oxidative N-Heterocyclic Carbene Catalysis,
A. Biswas, S. De Sarkar, L. Tebben, A. Studer,
Chem. Commun. 2012, 48, 5190-5192. [doi:10.1039/C2CC31501G]
144.
Hindered Biaryls by C-H Coupling: Bisoxazoline-Pd Catalysis Leading to Enantioselective C-H Coupling,
K. Yamaguchi, J. Yamaguchi, A. Studer, K. Itami,
Chem. Sci. 2012, 3, 2165-2169. [doi:10.1039/C2SC20277H]
143.
Structuring of Polymer Brushes and Surface Nitroxide Exchange Reactions,
H. Wagner, M. Becker, L. Chi, A. Studer,
in ACS Symposium Series, K. Matyjaszewski, B. S. Sumerlin, N. V. Tsaevsky (Eds.) 2012, 241-256. [doi:10.1021/bk-2012-1101.ch016]
142.
Radical Arylations,
S. E. Vaillard, A. Studer,
in Encyclopedia of Radicals in Chemistry, Biology and Materials, C. Chatgilialoglu, A. Studer (Eds.), Wiley 2012. [doi:10.1002/9781119953678.rad032]
141.
Controlled Nitroxide Mediated Radical Polymerization of Methyl and Phenyl Vinyl Ketone,
J. A. M. Hepperle, H. Luftmann, A. Studer,
J. Polym. Sci. Part A: Polym. Chem. 2012, 50, 2150-2160. [doi:10.1002/pola.25997]
140.
Oxidative Heck Arylation for the Stereoselective Synthesis of Tetrasubstituted Olefins Using Nitroxides as Oxidants,
Z. He, S. Kirchberg, R. Fröhlich, A. Studer,
Angew. Chem. Int. Ed. 2012, 51, 3699-3702. [doi:10.1002/anie.201108211];
highlighted in Synfacts 2012, 8, 709.
139.
Mechanistic Studies on the Pd-catalyzed Direct C-H Arylation of 2-Substituted Thiophene Derivatives with Arylpalladium Bipyridyl Complexes,
M. Steinmetz, K. Ueda, S. Grimme, J. Yamaguchi, S. Kirchberg, K. Itami, A. Studer,
Chem. Asian J. 2012, 7, 1256-1260. [doi:10.1002/asia.201101011]
138.
Encyclopedia of Radicals in Chemistry, Biology and Materials,
C. Chatgilialoglu, A. Studer (Eds.),
Wiley 2012. [doi:10.1002/9781119953678]
 
137.
Bis(phosphoryl)-Bridged Biphenyls by Radical Phosphanylation: Synthesis and Photophysical and Electrochemical Properties,
A. Bruch, A. Fukazawa, E. Yamaguchi, S. Yamaguchi, A. Studer,
Angew. Chem. Int. Ed. 2011, 50, 12094-12098. [doi:10.1002/anie.201104114]
136.
Amination of Benzoxazoles and 1,3,4-Oxadiazoles Using 2,2,6,6-Tetramethylpiperidine-N-oxoammonium Tetrafluoroborate as an Organic Oxidant,
S. Wertz, S. Kodama, A. Studer,
Angew. Chem. Int. Ed. 2011, 50, 11511-11515. [doi:10.1002/anie.201104735]
135.
Transition-Metal-Free TEMPO Catalyzed Oxidative Cross Coupling of Nitrones with Alkynyl Grignard Reagents,
S. Murarka, A. Studer,
Adv. Synth. Catal. 2011, 353, 2708-2714. [doi:10.1002/adsc.201100327]
134.
Formation of Isoxazolidines by Enantioselective Copper-Catalyzed Annulation of 2-Nitrosopyridine with Allylstannanes,
I. Chatterjee, R. Fröhlich, A. Studer,
Angew. Chem. Int. Ed. 2011, 50, 11257-11260. [doi:10.1002/anie.201105515];
highlighted in Synfacts 2011, 7, 177.
133.
Site Specific Protein Immobilization into Structured Polymer Brushes Prepared by AFM Lithography,
H. Wagner, Y. Li, M. Hirtz, L. Chi, H. Fuchs, A. Studer,
Soft Matter 2011, 7, 9854-9858. [doi:10.1039/C1SM06013A]
132.
One Product; Two Pathways - Initially Divergent Radical Reactions Can Reconverge to Form a Single Product in High Yield,
A. Bruch, R. Fröhlich, S. Grimme, A. Studer, D. P. Curran,
J. Am. Chem. Soc. 2011, 133, 16270-16276. [doi:10.1021/ja2070347]
131.
Highly Stereoselective Synthesis of 1,2,3-Trisubstituted Indanes via Oxidative N-Heterocyclic Carbene-Catalyzed Cascades,
A. Biswas, S. De Sarkar, R. Fröhlich, A. Studer,
Org. Lett. 2011, 13, 4966-4969. [doi:10.1021/ol202108a]
130.
Stereospecific Palladium-Catalyzed Decarboxylative C(sp3)-C(sp2) Coupling of 2,5-Cyclohexadiene-1-carboxylic Acid Derivatives with Aryl Iodides,
C.-M. Chou, I. Chatterjee, A. Studer,
Angew. Chem. Int. Ed. 2011, 50, 8614-8617. [doi:10.1002/anie.201103450];
showcased as Back Cover.
129.
Chemical Surface Modification of Self Assembled Monolayers by Radical Nitroxide Exchange Reactions,
H. Wagner, M. K. Brinks, M. Hirtz, A. Schäfer, L. Chi, A. Studer,
Chem. Eur. J. 2011, 17, 9107-9112. [doi:10.1002/chem.201100543]
128.
Kinetic Resolution of Secondary Alcohols by NHC Catalyzed Oxidative Esterification,
S. De Sarkar, A. Biswas, C. H. Song, A. Studer,
Synthesis 2011, 12, 1974-1983. [doi:10.1055/s-0030-1260030]
127.
Nitroxides: Applications in Synthesis and in Polymer Chemistry,
L. Tebben, A. Studer,
Angew. Chem. Int. Ed. 2011, 50, 5034-5068. [doi:10.1002/anie.201002547];
showcased as Inside Cover.
126.
Organocatalysis and C-H Activation Meet Radical- and Electron-Transfer Reactions,
A. Studer, D. P. Curran,
Angew. Chem. Int. Ed. 2011, 50, 5018-5022. [doi:10.1002/anie.201101597]
125.
Zinc Triflate Catalyzed Aerobic Cross-Dehydrogenative Coupling (CDC) of Alkynes with Nitrones: a New Entry to Isoxazoles,
S. Murarka, A. Studer,
Org. Lett. 2011, 13, 2746-2749. [doi:10.1021/ol200849k]
124.
Radical Alkylphosphanylation of Olefins with Stannylated or Silylated Phosphanes and Alkyl Iodides,
M.-C. Lamas, A. Studer,
Org. Lett. 2011, 13, 2236-2239. [doi:10.1021/ol200483p]
123.
Nitroxide-mediated Copolymerization of MMA with Styrene - Sequence Analysis of Oligomers by Using Mass Spectrometry,
I. C. Wienhöfer, H. Luftmann, A. Studer,
Macromolecules 2011, 44, 2510-2523. [doi:10.1021/ma1029482]
122.
Carboaminooxylation as a Tool to Prepare Functionalised Polymeric Materials: Introduction of Biologically Important Residues via Metal-free Radical C-C Coupling Reactions,
J.-P. Lindner, A. Studer,
Chem. Eur. J. 2011, 17, 4090-4094. [doi:10.1002/chem.201003163]
121.
Radical Transfer Hydroamination of Olefins with N-Aminated Dihydropyridines,
C.-M. Chou, J. Guin, C. Mück-Lichtenfeld, S. Grimme, A. Studer,
Chem. Asian J. 2011, 6, 1197-1209. [doi:10.1002/asia.201000881]
120.
Site-Specific Immobilization of Proteins at Zeolite L Crystals by Nitroxide Exchange Reactions,
M. Becker, L. De Cola, A. Studer,
Chem. Commun. 2011, 47, 3392-3394. [doi:10.1039/C0CC05474G]
119.
Aggregation Behaviour of Peptide-Polymer Conjugates Containing Linear Peptide Backbones and Multiple Polymer Side Chains,
M. Möller, C. Hentschel, L. Chi, A. Studer,
Org. Biomol. Chem. 2011, 9, 2403-2412. [doi:10.1039/C0OB01047B]
118.
Oxidative Biaryl Coupling of Thiophenes and Thiazoles with Arylboronic Acids through Palladium Catalysis: Otherwise Difficult C4-Selective C-H Arylation Enabled by Boronic Acids,
S. Kirchberg, S. Tani, K. Ueda, J. Yamaguchi, A. Studer, K. Itami,
Angew. Chem. Int. Ed. 2011, 50, 2387-2391. [doi:10.1002/anie.201007060];
highlighted in Synfacts 2011, 7, 537.
117.
Hydroxylamine as a source for nitric oxide in metal-free TEMPO catalyzed aerobic oxidation of alcohols,
S. Wertz, A. Studer,
Adv. Synth. Catal. 2011, 353, 69-72. [doi:10.1002/adsc.201000703]
116.
Patterning of proteins into nanostripes on Si-wafer over large areas: A combination of Langmuir-Blodgett patterning and orthogonal surface chemistry,
Y. Li, J. C. Niehaus, Y. Chen, H. Fuchs, A. Studer, H.-J. Galla, L. Chi,
Soft Matter 2011, 7, 861-863. [doi:10.1039/C0SM00994F]
 
115.
Synthesis of Macro(alkoxyamines) via Hydroboration of Poly(olefins) with Subsequent Nitroxide Oxidation for the Controlled Nitroxide Mediated Polymerization,
C. B. Wagner, A. Studer,
Macrom. Chem. & Physics 2010, 211, 2510-2516. [doi:10.1002/macp.201000420]
114.
NHC-Catalyzed Michael Addition to α,β-Unsaturated Aldehydes by Redox Activation,
S. De Sarkar, A. Studer,
Angew. Chem. Int. Ed. 2010, 49, 9266-9269. [doi:10.1002/anie.201004593]
113.
Oxidation of Alkylcatecholboranes with Functionalized Nitroxides for Chemical Modification of Cyclohexene, Perallylated Polyglycerol and of Poly(butadiene),
C. B. Wagner, A. Studer,
Eur. J. Org. Chem. 2010, 5782-5786. [doi:10.1002/ejoc.201001043]
112.
Patterning of Functional Compounds by Multi-component Langmuir-Blodgett Transfer and Subsequent Chemical Modification,
J. C. Niehaus, M. Hirtz, M. K. Brinks, A. Studer, H. Fuchs, L. Chi,
Langmuir 2010, 26, 15388-15393. [doi:10.1021/la102881r]
111.
Radical Addition of Arylboronic Acids to Various Olefins under Oxidative Conditions,
A. Dickschat, A. Studer,
Org. Lett. 2010, 12, 3972-3974. [doi:10.1021/ol101818k];
highlighted in Synfacts 2010, 6, 1411.
110.
Transition-Metal-Free Sonogashira-Type Coupling of Aryl and Alkynyl Grignard Reagents by Using TEMPO as an Oxidant,
M. S. Maji, S. Murarka, A. Studer,
Org. Lett. 2010, 12, 3878-3881. [doi:10.1021/ol1015702];
highlighted in Synfacts 2010, 6, 1401.
109.
1,2,3-Trisubstituted Indanes by Highly Diastereoselective Palladium-Catalyzed Oxyarylation of Indenes with Arylboronic Acids and Nitroxides,
S. Kirchberg, R. Fröhlich, A. Studer,
Angew. Chem. Int. Ed. 2010, 49, 6877-6880. [doi:10.1002/anie.201002214];
highlighted in Synfacts 2010, 6, 1260.
108.
Dynamic Microcrystal Assembly by Nitroxide Exchange Reactions,
B. Schulte, M. Tsotsalas, M. Becker, A. Studer, L. De Cola,
Angew. Chem. Int. Ed. 2010, 49, 6881-6884. [doi:10.1002/anie.201002851]
107.
Memory of Axial Chirality in Aryl Radical Phosphanylations,
A. Bruch, A. Ambrosius, R. Fröhlich, A. Studer, D. B. Guthrie, H. Zhang, D. P. Curran,
J. Am. Chem. Soc. 2010, 132, 11452-11454. [doi:10.1021/ja105070k]
106.
Transition Metal Free Synthesis of Conjugated Polymers from Bis-Grignard Reagents by Using TEMPO as Oxidant,
M. S. Maji, T. Pfeifer, A. Studer,
Chem. Eur. J. 2010, 16, 5872-5875. [doi:10.1002/chem.201000236]
105.
Copper Catalyzed Enantioselective [2+2] Cycloadditions of 2-Nitrosopyridine with Ketenes,
I. Chatterjee, C. Kumar Jana, M. Steinmetz, S. Grimme, A. Studer,
Adv. Synth. Catal. 2010, 352, 945-948. [doi:10.1002/adsc.201000153]
104.
Radical Amination with Trimethylstannylated Benzophenone Imine,
M.-C. Lamas, S. E. Vaillard, B. Wibbeling, A. Studer,
Org. Lett. 2010, 12, 2072-2075. [doi:10.1021/ol1005455]
103.
Oxidative Amidation and Azidation of Aldehydes by NHC Catalysis,
S. De Sarkar,A. Studer,
Org. Lett. 2010, 12, 1992-1995. [doi:10.1021/ol1004643]
102.
Poly(vinyl ketone)s by Controlled Boron Group Transfer Polymerization (BGTP),
K. Uehara, C. B. Wagner, T. Vogler, H. Luftmann, A. Studer,
Angew. Chem. Int. Ed. 2010, 49, 3073-3076. [doi:10.1002/anie.200907163];
highlighted in Synfacts 2010, 6, 658; highlighted in Nach. Chem. 2010, 58, 628.
101.
Immobilization of TEMPO Derivatives in Saponite and Use of these Novel Hybrid Materials as Reusable Catalysts,
C. Röben, A. Studer, Wilhelm L. Hemme, H. Eckert,
Synlett 2010, 1110-1114. [doi:10.1055/s-0029-1219587]
100.
NHC Catalyzed Oxidations of Aldehydes to Esters: Chemoselective Acylation of Alcohols in Presence of Amines,
S. De Sarkar, S. Grimme, A. Studer,
J. Am. Chem. Soc. 2010, 132, 1190-1191. [doi:10.1021/ja910540j];
highlighted in Synfacts 2010, 6, 359.
 
99.
Reusable Catalysts Based on Dendrimers Trapped in Poly(p-xylylene) Nanotubes,
J.-P. Berkan Lindner, C. Röben, A. Studer, M. Stasiak, R. Ronge, A. Greiner, H.-J. Wendorff,
Angew. Chem. Int. Ed. 2009, 48, 8874-8877. [doi:10.1002/anie.200903448];
highlighted in Synfacts 2010, 6, 107.
98.
Enantioselective Nitroso Diels-Alder Reaction and its Application for the Synthesis of Peracetylated (-)-Conduramine-A-1,
C. K. Jana, S. Grimme, A. Studer,
Chem. Eur. J. 2009, 15, 9078-9084. [doi:10.1002/chem.200901331]
97.
Oxidation of Catecholboron Enolates with TEMPO,
M. Pouliot, P. Renaud, K. Schenk, A. Studer, T. Vogler,
Angew. Chem. Int. Ed. 2009, 48, 6037-6040. [doi:10.1002/anie.200902242];
selected as Hot Paper, highlighted in Chimia.
96.
Transition-Metal-Free Oxidative Homocoupling of Aryl, Alkenyl, and Alkynyl Grignard Reagents with TEMPO,
M. S. Maji, A. Studer,
Synthesis 2009, 2467-2470. [doi:10.1055/s-0029-1216859]
95.
Microflow Radical Carboaminoxylations with a Novel Alkoxyamine,
I. C. Wienhöfer, A. Studer. M. T. Rahman, T. Fukuyama, I. Ryu,
Org. Lett. 2009, 11, 2457-2460. [doi:10.1021/ol900713d]
94.
Stereoselective Palladium-Catalyzed Carboaminoxylations of Indoles with Arylboronic Acids and TEMPO,
S. Kirchberg, R. Fröhlich, A. Studer,
Angew. Chem. Int. Ed. 2009, 48, 4235-4238. [doi:10.1002/anie.200901072]
93.
Polymer Brushes by Nitroxide-Mediated Polymerization,
M. K. Brinks, A. Studer,
Macromol. Rapid. Commun. 2009, 30, 1043-1057. [doi:10.1002/marc.200800720]
92.
1-tert-Butyl-3,3,5,5-tetraalkyl-2-piperazinon-4-oxyls - Highly Efficient Nitroxides for Controlled Radical Polymerization,
S. Miele, P. Nesvadba, A. Studer,
Macromolecules 2009, 42, 2419-2427. [doi:10.1021/ma802600x]
91.
Structured Polymer Brushes by AFM Lithography,
M. Hirtz, M. K. Brinks, S. Miele, A. Studer, H. Fuchs, L. Chi,
Small 2009, 5, 919-923. [doi:10.1002/smll.200801339]
90.
Azurin–Poly(N-isopropylacrylamide) Conjugates by Site-Directed Mutagenesis and their Thermosensitive Behavior in Electron-Transfer Processes,
N. Rosenberger, A. Studer, N. Takatani, H. Nakajima, Y. Watanabe,
Angew. Chem. Int. Ed. 2009, 48, 1946-1949. [doi:10.1002/anie.200804440];
highlighted in Nach. Chem. 2009, 57, 497.
 
89.
Oxidative Homocoupling of Aryl, Alkenyl, and Alkynyl Grignard Reagents with TEMPO and Dioxygen,
M. S. Maji, T. Pfeiffer, A. Studer,
Angew. Chem. Int. Ed. 2008, 47, 9547-9550. [doi:10.1002/anie.200804197];
selected as Hot Paper.
88.
Directed Palladium-Catalyzed Oxidative C-H Arylation of (Hetero)Arenes with Arylboronic Acids by using TEMPO,
S. Kirchberg, T. Vogler, A. Studer,
Synlett 2008, 2841-2846. [doi:10.1055/s-0028-1083546]
87.
Biomimetic Carbene-Catalyzed Oxidations of Aldehydes Using TEMPO,
J. Guin, S. De Sarkar, S. Grimme, A. Studer,
Angew. Chem. Int. Ed. 2008, 47, 8727-8730. [doi:10.1002/anie.200802735];
highlighted in Synfacts 2009, 5, 26.
86.
Radical-Based Arylation Methods,
S. E. Vaillard, B. Schulte, A. Studer,
in Modern Arylation Methods; L. Ackermann (Eds.); Wiley-VCH: Weinheim 2008, 475-511.
85.
Nitroxyl Radicals (Nitroxides),
A. Studer, T. Vogler,
in Science of Syntheis, D. Enders, E. Schaumann, (Eds.); Georg Thieme: Stuttgart, New York 2008, 845-853.
84.
Atroposelective Radical Aryl Migration Reactions from Sulfur to Carbon,
B. Schulte,  R. Fröhlich, A. Studer,
Tetrahedron 2008, 64, 11852-11859. [doi:10.1016/j.tet.2008.08.111]
83.
Rhodium-Catalyzed Oxidative Homocoupling of Boronic Acids,
T. Vogler, A. Studer,
Adv. Synth. Catal. 2008, 350, 1963-1967. [doi:10.1002/adsc.200800300]
82.
Immobilization of Oligostyrene-Prolinol Conjugates into Polystyrene via Electrospinning and Applications of these Fibers in Catalysis,
C. Röben, M. Stasiak, B. Janza, A. Greiner, J. H. Wendorff, A. Studer,
Synthesis 2008, 2163-2168. [doi:10.1055/s-2008-1067146]
81.
Total Synthesis of (+)-trans-Dihydronarciclasine via a Catalytic Enantioselective Regiodivergent Nitroso Diels-Alder Reaction,
C. K. Jana, A. Studer,
Chem. Eur. J. 2008, 14, 6326-6328. [doi:10.1002/chem.200800903]
80.
Applications of TEMPO in Synthesis,
T. Vogler, A. Studer,
Synthesis 2008, 1979-1993. [doi:10.1055/s-2008-1078445]
79.
(2,6-Dimethoxy-1-methyl-2,5-cyclohexadien-1-yl) (1,1-dimethylethyl)dimethylsilane,
A. Studer, J. Guin,
in Electronic Encyclopedia of Reagents for Organic Synthesis (e-EROS); L. A. Paquette (Hrsg.); J. Wiley & Sons 2008.
78.
Desymmetrization of Metallated Cyclohexadienes with Chiral N-tert-Butanesulfinyl Imines,
M. S. Maji, R. Fröhlich, A. Studer,
Org. Lett. 2008, 10, 1847-1850. [doi:10.1021/ol800478q]
77.
Ag-Catalyzed Stereoselective Cyclohexadienyl Transfer - A Novel Entry into Arylphenylmethanols,
R. Umeda, A. Studer,
Org. Lett. 2008, 10, 993-996. [doi:10.1021/ol703080a]
76.
Oxidative Coupling of Aryl Boronic Acids with Arenes via Rh-catalyzed Direct C-H Arylation,
T. Vogler, A. Studer,
Org. Lett. 2008, 10, 129-131. [doi:10.1021/ol702659a]
75.
Thiol-Catalyzed Stereoselective Transfer Hydroamination of Olefins with N-Aminated Dihydropyridines,
J. Guin, R. Fröhlich, A. Studer,
Angew. Chem. Int. Ed. 2008, 47, 779-782. [doi:10.1002/anie.200703902]
 
74.
Reversible Switching of Substrate Activity of Poly-N-Isopropylacrylamide Peptide Conjugates,
K. Molawi, A. Studer,
Chem. Commun. 2007, 5173-5175. [doi:10.1039/B713083J]
73.
Divergent Reactions for Racemates: Catalytic, Enantioselective, and Regiodivergent Nitroso Diels–Alder Reactions,
C. K. Jana, A. Studer,
Angew. Chem. Int. Ed. 2007, 46, 6542-6544. [doi:10.1002/anie.200701631]
72.
Homolytic Substitution at Phosphorus for the Synthesis of Alkyl and Aryl Phosphanes,
S. E. Vaillard, C. Mück-Lichtenfeld, S. Grimme, A. Studer,
Angew. Chem. Int. Ed. 2007, 46, 6533-6536. [doi:10.1002/anie.200701650]
71.
Design of Polymer Nanofiber Systems for the Immobilization of Homogeneous Catalysts - Preparation and Leaching Studies,
M. Stasiak, C. Röben, N. Rosenberger, F. Schleth, A. Studer, A. Greiner, J. H. Wendorff,
Polymer 2007, 48, 5208-5218. [doi:10.1016/j.polymer.2007.07.006]
70.
Site-Selective Surface-Initiated Polymerization by Langmuir–Blodgett Lithography,
M. K. Brinks, M. Hirtz, L. Chi, H. Fuchs, A. Studer,
Angew. Chem. Int. Ed. 2007, 46, 5231-5233. [doi:10.1002/anie.200605020]
69.
Radical Transfer Hydroamination with Aminated Cyclohexadienes Using Polarity Reversal Catalysis: Scope and Limitations,
J. Guin, C. Mück-Lichtenfeld, S. Grimme, A. Studer,
J. Am. Chem. Soc. 2007, 129, 4498-4503. [doi:10.1021/ja0692581]
68.
Polymer Fibers as Carriers for Homogeneous Catalysts,
M. Stasiak, A. Studer, A. Greiner, J. H. Wendorff,
Chem. Eur. J. 2007, 13, 6150-6156. [doi:10.1002/chem.200601555]
67.
Desymmetrization of 1,4-Cyclohexadienyltriisopropoxysilane using Cu-Catalysis,
R. Umeda, A. Studer,
Org. Lett. 2007, 9, 2175-2178. [doi:10.1021/ol070689d]
66.
Chemical Surface Modification via Radical C-C-Bond Forming Reactions,
K. O. Siegenthaler, A. Schäfer, A. Studer,
J. Am. Chem. Soc. 2007, 129, 5826-5827. [doi:10.1021/ja0686716]
65.
Structural requirements for optimized delivery, inhibition of oxidative stress and anti-apoptotic activity of targeted nitroxides,
J. Jiang, I. Kurnikov, N. A. Belikova, J. Xiao, Q. Zhao, I. L. Vlasova, A. A. Amoscato, R. Braslau, A. Studer, M. P. Fink, J. S. Greenberger, P. Wipf, V. E. Kagan,
J. Pharmacol. Exp. Ther 2007, 320, 1050-1060. [doi:10.1124/jpet.106.114769]
 
64.
A New Sterically Highly Hindered 7-Membered Cyclic Nitroxide for the Controlled Living Radical Polymerization,
C.-C. Chang, K. O. Siegenthaler, A. Studer,
Helv. Chim. Acta 2006, 89, 2200-2210. [doi:10.1002/hlca.200690206]
63.
The Effect of Additives on TEMPO-mediated Alkoxyamine Isomerizations: Experiments and Simulations,
T. Vogler, A. Studer,
Synthesis 2006, 4257-4265. [doi:10.1055/s-2006-950321]
62.
Radical Carboaminoxylation with Subsequent Pd-Catalyzed Intramolecular Allylation for the Construction of 5- and 6-Membered Carbocycles,
B. Schulte, A. Studer,
Synthesis 2006, 2129-2138. [doi:10.1055/s-2006-942416]
61.
Acceleration of the Styryl-TEMPO Mediated Controlled Radical Styrene-Polymerization by Addition of an Efficient Alkoxyamine,
C.-C. Chang, A. Studer,
Macromolecules 2006, 39, 4062-4068. [doi:10.1021/ma060068k]
60.
2,2,6,6-Tetramethylpiperidin-1-oxyl (TEMPO),
A. Studer, T. Vogler,
in Electronic Encyclopedia of Reagents for Organic Synthesis (e-EROS); L. A. Paquette (Hrsg.); J. Wiley & Sons 2006.
59.
Isonitrile Trapping Reactions under Thermolysis of Alkoxyamines for the Synthesis of Quinolines,
B. Janza, A. Studer,
Org. Lett. 2006, 8, 1875-1878. [doi:10.1021/ol0604421]
58.
Nitroxide-Mediated Radical Polymerization / Increase of Steric Demand in Nitroxides - How Much Is Too Much?,
K. O. Siegenthaler, A. Studer,
Macromolecules 2006, 39, 1347-1352. [doi:10.1021/ma0513463]
 
57.
Desymmetrization and Diastereotopic Group Selection in 1,4-Cyclohexadienes,,
A. Studer, F. Schleth,
Synlett 2005, 3033-3041. [doi:10.1055/s-2005-921899]
56.
A New Method for the Generation of Titanium(III)-Complexes and its Application in Pinacol Coupling Reactions,
C. A. Knoop, A. Studer,
Adv. Synth. Catal. 2005, 347, 1542-1546. [doi:10.1002/adsc.200505180]
55.
Evolution of functional cyclohexadiene-based synthetic reagents: the importance of becoming aromatic,
J. C. Walton, A. Studer,
Acc. Chem. Res. 2005, 38, 794-802. [doi:10.1021/ar050089j]
54.
Stereoselective Cyclization Reactions of IBX-generated Alkoxyamidyl Radicals,
B. Janza, A. Studer,
J. Org. Chem. 2005, 70, 6991-6994. [doi:10.1021/jo0509399]
53.
Nitroxide-Mediated Polymerization of N-Isopropylacrylamide - ESI-MS, MALDI-MS and MALLS Studies on Nitroxide-terminated PNIPAM´s,
T. Schulte, K. O. Siegenthaler, H. Luftmann, M. Letzel, A. Studer,
Macromolecules 2005, 38, 6833-6840. [doi:10.1021/ma050343n]
52.
Stabile Reagentien für die Erzeugung N-zentrierter Radikale: Hydroaminierung von Norbornenen,
J. Kemper, A. Studer,
Angew. Chem. Int. Ed. 2005, 44, 4914-4917. [doi:10.1002/anie.200463032]
51.
CO-Trapping Reaction under Thermolysis of Alkoxyamines - Application to the Synthesis of 3,4-Cyclopenta-1-Tetralone,
Y. Uenoyama, M. Tsukida, T. Doi, I. Ryu, A. Studer,
Org. Lett. 2005, 7, 2985-2988. [doi:10.1021/ol050951n]
50.
1,3-Dithiane-Derived Alkoxyamines as One-Carbon Radical Precursors,
A. J. Herrera, A. Studer,
Synthesis 2005, 1389-1396. [doi:10.1055/s-2005-865288]
49.
Nitroxide-mediated radical processes,
A. Studer, T. Schulte,
Chem. Rec. 2005, 5, 27-35. [doi:10.1002/tcr.20033]
48.
Tin-Free Radical Alkoxyamine Addition and Isomerization Reactions by Using the Persistent Radical Effect - Variation of the Alkoxyamine Structure,
K. Molawi, T. Schulte, K. O. Siegenthaler, C. Wetter, A. Studer,
Chem. Eur. J. 2005, 11, 2335-2350. [doi:10.1002/chem.200400936]
 
47.
One-Pot Homolytic Aromatic Substitons/HWE-Olefinations under Microwave Conditions for the Formation of a Small Oxindole Library,
A. Teichert, K. Jantos, K. Harms, A. Studer,
Org. Lett. 2004, 6, 3477-3480. [doi:10.1021/ol048759t]
46.
Stereocontrolled Formation of Vinylsilanes via Homolytic Substitution at Silicon,
A. Blum, W. Hess, A. Studer,
Synthesis 2004, 2226-2235. [doi:10.1055/s-2004-829186]
45.
Stereoselective Synthesis of (+)-Nephrosteranic Acid, (+)-trans-Cognac Lactone and (+)-trans-Whisky Lactone using a Chiral Cyclohexadienyl-Ti-Compound,
F. Schleth, T. Vogler, K. Harms, A. Studer,
Chem. Eur. J. 2004, 10, 4171-4185. [doi:10.1002/chem.200400237]
44.
Nitroxide Mediated Living Free Radical Polymerization of Styrene - A Systematic Study of the Variation of the Alkoxyamine Concentration,
T. Schulte, C. A. Knoop, A. Studer,
J. Polym. Sci., Part A: Polym. Chem. 2004, 42, 3342-3351. [doi:10.1002/pola.20177]
43.
Tin-Free Radical Chemistry Using The Persistent Radical Effect: Alkoxyamine Isomerization, Addition Reactions and Polymerizations,
A. Studer,
Chem. Soc. Rev. 2004, 33, 267-273. [doi:10.1039/B307652K]
42.
Steric and Electronic Effects in Cyclic Alkoxyamines - Synthesis and Applications as Regulators for the Controlled/Living Radical Polymerization,
C. Wetter, J. Gierlich ,C. A. Knoop, C. Müller, T. Schulte, A. Studer,
Chem. Eur. J. 2004, 10, 1156-1166. [doi:10.1002/chem.200305427]
41.
New Sterically Hindered Nitroxides for the Living Free Radical Polymerization:  X-ray Structure of an α-H-Bearing Nitroxide,
A. Studer, K. Harms, C. Knoop, C. Müller, T. Schulte,
Macromolecules 2004, 37, 27-34. [doi:10.1021/ma035128q]
40.
Microwave-assisted Free Radical Chemistry using the Persistent Radical Effect,
C. Wetter, A. Studer,
Chem. Commun. 2004, 174-175. [doi:10.1039/B313139D]
 
39.
Hydroxy- and Silyloxy-Substituted TEMPO-Derivatives for the Living Free Radical Polymerization of Styrene and n-Butyl Acrylate: Synthesis, Kinetics and Mechanistic Studies,
C. A. Knoop, A. Studer,
J. Am. Chem. Soc. 2003, 125, 16327-16333. [doi:10.1021/ja037948o]
38.
Intermolecular Radical Addition/Cyclization Reactions of Alkoxyamines onto Nonactivated Alkenes,
C. Wetter, K. Jantos, K. Woithe, A. Studer,
Org. Lett. 2003, 5, 2899-2902. [doi:10.1021/ol034994k]
37.
Silylated Cyclohexadienes as New Radical Chain Reducing Reagents: Preparative and Mechanistic Aspects,
A. Studer, S. Amrein, F. Schleth, T. Schulte, J. C. Walton,
J. Am. Chem. Soc. 2003, 125, 5726-5733. [doi:10.1021/ja0341743]
36.
Two types of intramolecular homolytic substitution reactions at group XIV atoms: unusual radical 1,4-Sn shifts from Si to C and carbonylative SHi reaktion at Si,
A. Studer, S. Amrein, H. Matsubara, C. H. Schiesser, T. Doi, T. Kawamura, T. Fukuyama, I. Ryu,
Chem. Commun. 2003, 1190-1191. [doi:10.1039/B301755A]
35.
New Seven- and Eight-membered cyclic alkoxyamines for the living free radical polymerization,
T. Schulte, A. Studer,
Macromolecules 2003, 36, 3078-3084. [doi:10.1021/ma025806t]
34.
Desymmetrization of Metalated Cyclohexadienes and Application to the Synthesis of Nephrosteranic Acid,
F. Schleth, A. Studer,
Angew. Chem. Int. Ed. 2003, 43, 313-315. [doi:10.1002/anie.200352254]
 
33.
Silylated Cyclohexadienes in Radical Chain Hydrosilylations,
S. Amrein, A. Studer,
Helv. Chim. Acta 2002, 85, 3559-3574. [doi:10.1002/1522-2675(200210)85:10<3559::AID-HLCA3559>3.0.CO;2-6]
32.
Stereoselective Electrophilic Cyclisations of O-Homoallyl-Hydroxylamine Derivatives,
B. Janza, A. Studer,
Synthesis 2002, 2117-2123. [doi:10.1055/s-2002-34385]
31.
Stereoselective Radical Aryl Migration Reactions from Sulfur to Carbon,
M. Bossart, R. Fässler, J. Schoenberger, A. Studer,
Eur. J. Org. Chem. 2002, 2742-2757. [doi:10.1002/1099-0690(200208)2002:16<2742::AID-EJOC2742>3.0.CO;2-R]
30.
Intramolecular radical hydrosilylation - the first radical 5-endo-dig cyclisation,
S. Amrein, A. Studer,
Chem. Commun. 2002, 1592-1593. [doi:10.1039/B204879E]
29.
Tin Hydride Substitutes in Reductive Radical Chain Reactions,
A. Studer, S. Amrein,
Synthesis 2002, 835-849. [doi:10.1055/s-2002-28507]
 
28.
Radical Aryl Migration Reactions,
A. Studer, M. Bossart,
Tetrahedron 2001, 57, 9649-9667. [doi:10.1016/S0040-4020(01)00990-5]
27.
Radical Transfer Hydrosilylation/Cyclization Using Silylated Cyclohexadienes,
S. Amrein, A. Timmermann, A. Studer,
Org. Lett. 2001, 3, 2357-2360. [doi:10.1021/ol016160c]
26.
The Persistent Radical Effect in Organic Synthesis,
A. Studer,
Chem. Eur. J. 2001, 7, 1159-1164. [doi:10.1002/1521-3765(20010316)7:6<1159::AID-CHEM1159>3.0.CO;2-I]
25.
Trendberichte 2000 - Radikalchemie,
A. Studer,
Nachr. Chem. 2001, 49, 300-305. [doi:10.1002/nadc.20010490308]
24.
Factors Influencing the C-O-Bond Homolysis of Alkoxyamines: Effects of H-Bonding and Polar Substituents,
S. Marque, H. Fischer, E. Baier, A. Studer,
J. Org. Chem. 2001, 66, 1146-1156. [doi:10.1021/jo001190z]
23.
Aromatic Substitution,
A. Studer, M. Bossart,
in Radicals in Organic Synthesis, Vol. 2; P. Renaud, M. Sibi, Eds; Wiley-VCH: Weinheim 2001, 62-80. [doi:10.1002/9783527618293]
 
22.
Experimental Techniques in Fluorous Synthesis: A User's Guide,
D. P. Curran, S. Hadida, A. Studer, M. He, S.-Y. Kim, Z. Luo, M. Larhed, A. Hallberg, B. Linclau,
in Combinatorial Chemistry: A Practical Approach; H. Fenniri, Ed.; Oxford Univ. Press 2000, 327-352.
21.
Silylated Cyclohexadienes: New Alternatives to Tributyltin Hydride in Free Radical Chemistry,
A. Studer, S. Amrein,
Angew. Chem. Int. Ed. 2000, 39, 3080-3082. [doi:10.1002/1521-3773(20000901)39:17<3080::AID-ANIE3080>3.0.CO;2-E]
20.
Stereoselective Radical Aryl Migration from Silicon to Carbon,
S. Amrein, M. Bossart, T. Vasella, A. Studer,
J. Org. Chem. 2000, 65, 4281-4288. [doi:10.1021/jo000041d]
19.
Tin-Free Radical Cyclization Reactions Using the Persistent Radical Effect,
A. Studer,
Angew. Chem. Int. Ed. 2000, 39, 1108-1111. [doi:10.1002/(SICI)1521-3773(20000317)39:6<1108::AID-ANIE1108>3.0.CO;2-A]
18.
Synthesis of Biaryls by Intramolecular Radical Aryl Migration from Silicon to Carbon,
A. Studer, M. Bossart, T. Vasella,
Org. Lett. 2000, 2, 985-988. [doi:10.1021/ol005661f]
 
17.
The SHi Reaction at Silicon - A new Entry into Cyclic Alkoxysilanes,
A. Studer, H. Steen,
Chem. Eur. J. 1999, 5, 759-773. [doi:10.1002/(SICI)1521-3765(19990201)5:2<759::AID-CHEM759>3.0.CO;2-V]
 
16.
SHi Reactions at Silicon as Unimolecular Chain Transfer Steps in the Formation of Cyclic Alkoxysilanes,
A. Studer,
Angew. Chem. Int. Ed. 1998, 110, 507-510. [doi:10.1002/(SICI)1521-3773(19980302)37:4<462::AID-ANIE462>3.0.CO;2-M]
15.
Stereoselective Radical Aryl Migrations from Sulfur to Carbon,
A. Studer, M. Bossart,
Chem. Commun. 1998, 2127-2128. [doi:10.1039/A806718J ]
14.
Stereoselective Phenyl Migration from Silicon to Carbon,
A. Studer, M. Bossart, H. Steen,
Tetrahedron Lett. 1998, 39, 8829-8832. [doi:10.1016/S0040-4039(98)02045-0]
 
13.
Fluorous Synthesis: Fluorous Protocols for the Ugi and Biginelli Multi-Component Condensations,
A. Studer, P. Jeger, P. Wipf, D. P. Curran,
J. Org. Chem. 1997, 62, 2917-2924. [doi:10.1021/jo970095w]
12.
Fluorous Synthesis: A Fluorous-Phase Strategy for Improving Separation Efficiency in Organic Synthesis,,
A. Studer, S. Hadida, R. Ferritto, S.-Y. Kim, P. Jeger, P. Wipf, D. P. Curran,
Science 1997, 275, 823-826. [doi:10.1126/science.275.5301.823 ]
11.
A Strategic Alternative to Solid Phase Synthesis: Preparation of a Small Isoxazoline Library by "Fluorous Synthesis",
A. Studer, D. P. Curran,
Tetrahedron 1997, 53, 6681-6696. [doi:10.1016/S0040-4020(97)00224-X]
 
10.
Amino Acids and Their Derivatives as Stoichiometric Auxiliaries in Asymmetric Synthesis,
A. Studer,
Synthesis 1996, 793-815. [doi:10.1055/s-1996-4313]
9.
Reductive Coupling and Reductive Demethoxylation of Aromatic Dimethylacetals with SmI2/Trifluoroacetic Acid, SmI2/BF3·Et2O, or SmI2/H2O,
A. Studer, D. P. Curran,
Synlett 1996, 255-257. [doi:10.1055/s-1996-5389]
 
8.
Preparation of Either Enantiomer of 1,2-Diaminoalkane-2-phosphonic Acid Derivatives,
A. Studer, D. Seebach,
Heterocycles 1995, 40, 357-378. [doi:10.3987/COM-94-S44]
7.
Synthesis and First Applications of a New Chiral Auxiliary (tert-Butyl-2-(tert-Butyl)- 5,5-dimethyl-4-oxo imidazolidine-1-carboxylate,
A. Studer, T. Hintermann, D. Seebach,
Helv. Chim. Acta 1995, 78, 1185-1206. [doi:10.1002/hlca.19950780512]
6.
Some Effects of Lithium Salts, of Strong Bases, and of the Cosolvent DMPU in Peptide Chemistry, and Elsewhere,
D. Seebach, A. K. Beck, A. Studer,
in Modern Synthetic Methods; Vol. 7; B. Ernst, C. Leumann (Eds.); Verlag Helvetica Chimica Acta: Basel, VCH: Weinheim 1995, 1-178.
5.
Dissertation: Neue Anwendungen der 2-tert-Butylimidazolidinone in der asymmetrischen Synthese,
A. Studer,
ETH Zürich 1995. [doi:10.3929/ethz-a-001459663]
4.
t-Butyl 2-t-Butyl-3-methyl-4-oxo-1-imidazolidine carboxylate,
A. Studer, D. Seebach,
in Encyclopedia of Reagents for Organic Synthesis; Vol. 2; L. A. Paquette (Ed.-in-Chief); J. Wiley & Sons: Chichester 1995, 852-854.
3.
1-Benzoyl-2-t-butyl-3,5-dimethyl-4-imidazolidinone,
A. Studer, D. Seebach,
in Encyclopedia of Reagents for Organic Synthesis; Vol. 1; L. A. Paquette (Ed.-in-Chief); J. Wiley & Sons: Chichester 1995, 306-308.
2.
Enantioselective Synthesis of a Branched α-Amino Acids with Bulky Substituents,
A. Studer, D. Seebach,
Liebigs Ann. Chem. 1995, 217-222. [doi:10.1002/jlac.199519950231]
 
1.
Synthesis of Tri-, Penta- and Heptapeptides Containing an (R)-2-Alkyl-2-amino- 3-methyl aminopropionic Acid Residue in the Central Position,
D. Seebach, A. Studer, E. Pfammatter, H. Widmer,
Helv. Chim. Acta 1994, 77, 2035-2050. [doi:10.1002/hlca.19940770728]
 
Patent
(4).
1,4-Cyclohexadien funktionelle Organosiliciumverbindungen,
T. Kammel, B. Pachaly, R. Weidner, A. Studer, L. Alvarez-Garcia, A. Herrera-Gonzalez,
DE-Patent 10326577 A 2004.
Patent
(3).
Fluorous Reaction and Separation Systems,
D. P. Curran, S. Hadida, M. Hoshino, A. Studer, S.-Y. Kim, P. Wipf, P. Jäger,
US-Patent 6156896 2000.
Patent
(2).
Fluorous Reaction and Separation Systems,
D. P. Curran, S. Hadida, M. Hoshino, A. Studer, S.-Y. Kim, P. Wipf, P. Jäger,
US-Patent 5859247 1999.
Patent
(1).
Fluorous Reaction Systems ,
D. P. Curran, S. Hadida, A. Studer, M. Hoshino,
US-Patent 5777121 1998.