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Magnus Rueping - Publications

Affiliations: 
Rheinisch-Westfaelische Technische Hochschule, Aachen, NRW, Germany 
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334 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Kancherla R, Muralirajan K, Dutta S, Pal K, Li B, Maity B, Cavallo L, Rueping M. Photoexcitation of Distinct Divalent Palladium Complexes in Cross-Coupling Amination Under Air. Angewandte Chemie (International Ed. in English). e202314508. PMID 37956272 DOI: 10.1002/anie.202314508  0.814
2023 Muralirajan K, Kancherla R, Maity B, Karuthedath S, Laquai F, Cavallo L, Rueping M. Mechanistic insights into excited-state palladium catalysis for C-S bond formations and dehydrogenative sulfonylation of amines. Nature Communications. 14: 6622. PMID 37857662 DOI: 10.1038/s41467-023-42392-2  0.759
2023 Zhang J, Rueping M. Metallaphotoredox catalysis for sp C-H functionalizations through hydrogen atom transfer (HAT). Chemical Society Reviews. PMID 37278288 DOI: 10.1039/d3cs00023k  0.334
2023 Xing L, Yang Q, Zhu C, Bai Y, Tang Y, Rueping M, Cai Y. Poly(heptazine imide) ligand exchange enables remarkable low catalyst loadings in heterogeneous metallaphotocatalysis. Nature Communications. 14: 1501. PMID 36932064 DOI: 10.1038/s41467-023-37113-8  0.651
2023 Huang L, Szewczyk M, Kancherla R, Maity B, Zhu C, Cavallo L, Rueping M. Modulating stereoselectivity in allylic C(sp)-H bond arylations via nickel and photoredox catalysis. Nature Communications. 14: 548. PMID 36725849 DOI: 10.1038/s41467-023-36103-0  0.757
2023 Long T, Zhu C, Li L, Shao L, Zhu S, Rueping M, Chu L. Ligand-controlled stereodivergent alkenylation of alkynes to access functionalized trans- and cis-1,3-dienes. Nature Communications. 14: 55. PMID 36599820 DOI: 10.1038/s41467-022-35688-2  0.306
2022 Li B, Wang K, Yue H, Drichel A, Lin J, Su Z, Rueping M. Catalyst-Free C(sp)-H Borylation through Aryl Radical Generation from Thiophenium Salts via Electron Donor-Acceptor Complex Formation. Organic Letters. PMID 36191259 DOI: 10.1021/acs.orglett.2c03008  0.408
2022 Kumar GS, Shinde PS, Chen H, Muralirajan K, Kancherla R, Rueping M. Paired Electrolysis for Decarboxylative Cyanation: 4-CN-Pyridine, a Versatile Nitrile Source. Organic Letters. PMID 36036921 DOI: 10.1021/acs.orglett.2c01897  0.773
2022 Kancherla R, Muralirajan K, Rueping M. Excited-state palladium-catalysed reductive alkylation of imines: scope and mechanism. Chemical Science. 13: 8583-8589. PMID 35974758 DOI: 10.1039/d2sc02363f  0.759
2022 Zhu C, Lee SC, Chen H, Yue H, Rueping M. Reductive Cross-Coupling of α-Oxy Halides Enabled by Thermal Catalysis, Photocatalysis, Electrocatalysis, or Mechanochemistry. Angewandte Chemie (International Ed. in English). e202204212. PMID 35816102 DOI: 10.1002/anie.202204212  0.308
2022 Sagadevan A, Ghosh A, Maity P, Mohammed OF, Bakr OM, Rueping M. Visible-Light Copper Nanocluster Catalysis for the C-N Coupling of Aryl Chlorides at Room Temperature. Journal of the American Chemical Society. PMID 35766900 DOI: 10.1021/jacs.2c02218  0.38
2022 Chen H, Yue H, Zhu C, Rueping M. Reactivity in Nickel-Catalyzed Multi-component Sequential Reductive Cross-Coupling Reactions. Angewandte Chemie (International Ed. in English). e202204144. PMID 35727897 DOI: 10.1002/anie.202204144  0.367
2022 Zhu C, Yue H, Rueping M. Nickel catalyzed multicomponent stereodivergent synthesis of olefins enabled by electrochemistry, photocatalysis and photo-electrochemistry. Nature Communications. 13: 3240. PMID 35688818 DOI: 10.1038/s41467-022-30985-2  0.368
2022 Kancherla R, Muralirajan K, Maity B, Karuthedath S, Kumar GS, Laquai F, Cavallo L, Rueping M. Mechanistic insights into photochemical nickel-catalyzed cross-couplings enabled by energy transfer. Nature Communications. 13: 2737. PMID 35585041 DOI: 10.1038/s41467-022-30278-8  0.759
2022 Magre M, Szewczyk M, Rueping M. s-Block Metal Catalysts for the Hydroboration of Unsaturated Bonds. Chemical Reviews. PMID 35254061 DOI: 10.1021/acs.chemrev.1c00641  0.736
2021 Yue H, Zhu C, Huang L, Dewanji A, Rueping M. Advances in allylic and benzylic C-H bond functionalization enabled by metallaphotoredox catalysis. Chemical Communications (Cambridge, England). 58: 171-184. PMID 34882164 DOI: 10.1039/d1cc06285a  0.71
2021 Zhu C, Zhumagazy S, Yue H, Rueping M. Metal-free C-Se cross-coupling enabled by photoinduced inter-molecular charge transfer. Chemical Communications (Cambridge, England). 58: 96-99. PMID 34874034 DOI: 10.1039/d1cc06152f  0.351
2021 Muralirajan K, Kancherla R, Gimnkhan A, Rueping M. Unactivated Alkyl Chloride Reactivity in Excited-State Palladium Catalysis. Organic Letters. 23: 6905-6910. PMID 34432470 DOI: 10.1021/acs.orglett.1c02467  0.752
2021 Zubar V, Dewanji A, Rueping M. Chemoselective Hydrogenation of Nitroarenes Using an Air-Stable Base-Metal Catalyst. Organic Letters. PMID 33754743 DOI: 10.1021/acs.orglett.1c00659  0.752
2021 Polishchuk I, Sklyaruk J, Lebedev Y, Rueping M. Air Stable Iridium Catalysts for Direct Reductive Amination of Ketones. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 33508154 DOI: 10.1002/chem.202005508  0.361
2020 Jia J, Kancherla R, Rueping M, Huang L. Allylic C(sp)-H alkylation synergistic organo- and photoredox catalyzed radical addition to imines. Chemical Science. 11: 4954-4959. PMID 34122952 DOI: 10.1039/d0sc00819b  0.78
2020 Zhu C, Yue H, Jia J, Rueping M. Recent Advances in Nickel-Catalyzed C-Heteroatom Cross-Coupling Reactions under Mild Conditions via Facilitated Reductive Elimination. Angewandte Chemie (International Ed. in English). PMID 33252192 DOI: 10.1002/anie.202013852  0.352
2020 Maity B, Zhu C, Yue H, Huang L, Harb M, Minenkov Y, Rueping M, Cavallo L. Mechanistic Insight into the Photoredox-Nickel-HAT Triple Catalyzed Arylation and Alkylation of α-Amino Csp3-H Bonds. Journal of the American Chemical Society. PMID 32900195 DOI: 10.1021/Jacs.0C05010  0.446
2020 Zhu C, Yue H, Chu L, Rueping M. Recent advances in photoredox and nickel dual-catalyzed cascade reactions: pushing the boundaries of complexity. Chemical Science. 11: 4051-4064. PMID 32864080 DOI: 10.1039/D0Sc00712A  0.456
2020 Sklyaruk J, Zubar V, Borghs JC, Rueping M. Methanol as the Hydrogen Source in the Selective Transfer Hydrogenation of Alkynes Enabled by a Manganese Pincer Complex. Organic Letters. 22: 6067-6071. PMID 32790430 DOI: 10.1021/Acs.Orglett.0C02151  0.434
2020 Magre M, Paffenholz E, Maity B, Cavallo L, Rueping M. Regiodivergent Hydroborative Ring Opening of Epoxides via Selec-tive C-O Bond Activation. Journal of the American Chemical Society. PMID 32658463 DOI: 10.1021/Jacs.0C05917  0.752
2020 Zubar V, Sklyaruk J, Brzozowska A, Rueping M. Chemoselective Hydrogenation of Alkynes to ()Alkenes Using an Air-Stable Base Metal Catalyst. Organic Letters. 22: 5423-5428. PMID 32639161 DOI: 10.1021/Acs.Orglett.0C01783  0.497
2020 Azofra LM, Tran MA, Zubar V, Cavallo L, Rueping M, El-Sepelgy O. Conversion of racemic alcohols to optically pure amine precursors enabled by catalyst dynamic kinetic resolution: experiment and computation. Chemical Communications (Cambridge, England). PMID 32638725 DOI: 10.1039/D0Cc02881A  0.79
2020 Borghs JC, Zubar V, Azofra LM, Sklyaruk J, Rueping M. Manganese-Catalyzed Regioselective Dehydrogenative C- versus N-Alkylation Enabled by a Solvent Switch: Experiment and Computation. Organic Letters. 22: 4222-4227. PMID 32401525 DOI: 10.1021/Acs.Orglett.0C01270  0.494
2020 Zubar V, Borghs JC, Rueping M. Hydrogenation or Dehydrogenation of N-Containing Heterocycles Catalyzed by a Single Manganese Complex. Organic Letters. PMID 32364749 DOI: 10.1021/Acs.Orglett.0C01273  0.452
2020 Krach PE, Dewanji A, Yuan T, Rueping M. Synthesis of unsymmetrical ketones by applying visible-light benzophenone/nickel dual catalysis for direct benzylic acylation. Chemical Communications (Cambridge, England). PMID 32352104 DOI: 10.1039/D0Cc01480J  0.792
2020 Rueping M, Shinde V, Mane M, Cavallo L. Iridium (I)-Catalyzed Enantioselective Hydroarylation of Alkenes via C-H bond Activation: Experiment and Computation. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32301132 DOI: 10.1002/Chem.202001793  0.515
2020 Brzozowska A, Zubar V, Ganardi RC, Rueping M. Chemoselective Hydroboration of Propargylic Alcohols and Amines Using a Manganese(II) Catalyst. Organic Letters. PMID 32227972 DOI: 10.1021/Acs.Orglett.0C00941  0.396
2020 Magre M, Szewczyk M, Rueping M. -Methylation and Trideuteromethylation of Amines via Magnesium-Catalyzed Reduction of Cyclic and Linear Carbamates. Organic Letters. PMID 32216366 DOI: 10.1021/Acs.Orglett.0C00988  0.753
2020 Ji T, Chen XY, Huang L, Rueping M. Remote Trifluoromethylthiolation Enabled by Organophotocatalytic C-C Bond Cleavage. Organic Letters. PMID 32176516 DOI: 10.1021/Acs.Orglett.0C00493  0.428
2020 Magre M, Szewczyk M, Rueping M. Magnesium-Catalyzed Stereoselective Hydrostannylation of Internal and Terminal Alkynes. Organic Letters. 22: 1594-1598. PMID 32023069 DOI: 10.1021/Acs.Orglett.0C00184  0.766
2020 Huang L, Ji T, Rueping M. Remote Nickel-Catalyzed Cross-Coupling Arylation via Proton-Coupled Electron Transfer-Enabled C-C Bond Cleavage. Journal of the American Chemical Society. PMID 32017543 DOI: 10.1021/Jacs.9B12490  0.391
2020 Gadde SK, Peshkov A, Brzozowska A, Nikolaienko P, Zhu C, Rueping M. Nickel catalyzed chain walking cross-ele ctrophile coupling of alkyl and aryl halides and olefin hydroarylation enabled by electrochemical reduction. Angewandte Chemie (International Ed. in English). PMID 32017340 DOI: 10.1002/Anie.201915418  0.464
2020 Dewanji A, Bülow RF, Rueping M. Photoredox/Nickel Dual-Catalyzed Reductive Cross Coupling of Aryl Halides Using an Organic Reducing Agent. Organic Letters. 22: 1611-1617. PMID 32011897 DOI: 10.1021/Acs.Orglett.0C00199  0.744
2020 Banala S, Zhu L, Himmel L, Merkes JM, Kiessling F, Rueping M. Atropisomers of meso tetra (N-mesyl pyrrol-2-yl) porphyrins: Synthesis, isolation and characterisation of all-pyrrolic porphyrins. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31943372 DOI: 10.1002/Chem.201905637  0.31
2020 Rueping M. Regioselective Hydroalkylation and Arylalkylation of Alkynes: Application and Mechanism. Angewandte Chemie (International Ed. in English). PMID 31901214 DOI: 10.1002/Anie.201914061  0.426
2020 Jia J, Kancherla R, Rueping M, Huang L. Allylic C(sp3)–H alkylation via synergistic organo- and photoredox catalyzed radical addition to imines Chemical Science. 11: 4954-4959. DOI: 10.1039/D0Sc00819B  0.768
2020 Jia J, Lefebvre Q, Rueping M. Reductive coupling of imines with redox-active esters by visible light photoredox organocatalysis Organic Chemistry Frontiers. 7: 602-608. DOI: 10.1039/C9Qo01428D  0.368
2020 Merkes JM, Lammers T, Kancherla R, Rueping M, Kiessling F, Banala S. Photoacoustic Imaging: Tuning Optical Properties of BODIPY Dyes by Pyrrole Conjugation for Photoacoustic Imaging (Advanced Optical Materials 11/2020) Advanced Optical Materials. 8: 2070046. DOI: 10.1002/Adom.202070046  0.682
2020 Merkes JM, Lammers T, Kancherla R, Rueping M, Kiessling F, Banala S. Tuning Optical Properties of BODIPY Dyes by Pyrrole Conjugation for Photoacoustic Imaging Advanced Optical Materials. 8: 1902115. DOI: 10.1002/Adom.201902115  0.694
2019 Ghosh M, Shinde VS, Rueping M. A review of asymmetric synthetic organic electrochemistry and electrocatalysis: concepts, applications, recent developments and future directions. Beilstein Journal of Organic Chemistry. 15: 2710-2746. PMID 31807206 DOI: 10.3762/Bjoc.15.264  0.341
2019 Huang L, Zhu C, Yi L, Yue H, Kancherla R, Rueping M. Cascade Cross-Coupling of Dienes: Photoredox and Nickel Dual Catalysis. Angewandte Chemie (International Ed. in English). PMID 31778289 DOI: 10.1002/Anie.201911109  0.764
2019 Lefebvre Q, Porta R, Millet A, Jia J, Rueping M. One Amine - 3 Tasks: Reductive Coupling of Imines with Olefins in Batch and Flow. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31777987 DOI: 10.1002/Chem.201904483  0.357
2019 Lee SC, Guo L, Rueping M. Nickel-catalyzed exo-selective hydroacylation/Suzuki cross-coupling reaction. Chemical Communications (Cambridge, England). PMID 31777905 DOI: 10.1039/C9Cc07558E  0.471
2019 Srimontree W, Lakornwong W, Rueping M. Nickel-Catalyzed Synthesis of Silanes from Silyl Ketones. Organic Letters. PMID 31702934 DOI: 10.1021/Acs.Orglett.9B03487  0.495
2019 Lebedev YN, Polishchuk I, Maity B, Cavallo L, Rueping M. Asymmetric Hydroboration of Heteroaryl Ketones by Aluminum Catalysis. Journal of the American Chemical Society. PMID 31701746 DOI: 10.1021/Jacs.9B10364  0.461
2019 Chatupheeraphat A, Rueping M, Magre M. Chemo- and Regioselective Magnesium-Catalyzed -Alkenylation of Anilines. Organic Letters. PMID 31668080 DOI: 10.1021/Acs.Orglett.9B03526  0.78
2019 Srimontree W, Guo L, Rueping M. Hydride Transfer Enables the Nickel-catalyzed ipso-Borylation and Silylation of Aldehydes Watchara Srimontree, Lin Guo and Magnus Rueping. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31660666 DOI: 10.1002/Chem.201904842  0.427
2019 Falconnet A, Magre M, Maity B, Cavallo L, Rueping M. Asymmetric Magnesium-Catalyzed Hydroboration by Metal-Ligand Cooperative Catalysis. Angewandte Chemie (International Ed. in English). PMID 31642572 DOI: 10.1002/Anie.201908012  0.768
2019 Kleinschmidt D, Fernandes MS, Mork M, Meyer AA, Krischel J, Anakhov MV, Gumerov RA, Potemkin II, Rueping M, Pich A. Enhanced catalyst performance through compartmentalization exemplified by colloidal l-proline modified microgel catalysts. Journal of Colloid and Interface Science. 559: 76-87. PMID 31610307 DOI: 10.1016/J.Jcis.2019.10.005  0.415
2019 Jang YK, Magre M, Rueping M. Chemoselective Luche-Type Reduction of α,β-Unsaturated Ketones by Magnesium Catalysis. Organic Letters. PMID 31588757 DOI: 10.1021/Acs.Orglett.9B03131  0.758
2019 Kalsi D, Barsu N, Chakrabarti S, Dahiya P, Rueping M, Sundararaju B. C-H and N-H bond annulation of aryl amides with unactivated olefins by merging cobalt(iii) and photoredox catalysis. Chemical Communications (Cambridge, England). PMID 31502608 DOI: 10.1039/C9Cc05744G  0.445
2019 Borghs JC, Tran MA, Sklyaruk J, Rueping M, El-Sepelgy O. Sustainable Alkylation of Nitriles with Alcohols by Manganese Catalysis. The Journal of Organic Chemistry. PMID 31116947 DOI: 10.1021/Acs.Joc.9B00792  0.805
2019 Yue H, Zhu C, Shen L, Geng Q, Hock KJ, Yuan T, Cavallo L, Rueping M. Nickel-catalyzed C-N bond activation: activated primary amines as alkylating reagents in reductive cross-coupling. Chemical Science. 10: 4430-4435. PMID 31057770 DOI: 10.1039/C9Sc00783K  0.435
2019 Guo L, Srimontree W, Zhu C, Maity B, Liu X, Cavallo L, Rueping M. Nickel-catalyzed Suzuki-Miyaura cross-couplings of aldehydes. Nature Communications. 10: 1957. PMID 31036821 DOI: 10.1038/S41467-019-09766-X  0.476
2019 Magre M, Maity B, Falconnet A, Cavallo L, Rueping M. Magnesium-Catalyzed Hydroboration of Terminal and Internal Alkynes. Angewandte Chemie (International Ed. in English). PMID 30977970 DOI: 10.1002/Anie.201902188  0.762
2019 Nikolaienko P, Jentsch M, Kale AP, Rueping M. Electrochemical and scalable dehydrogenative C(sp3)-H amination via remote hydrogen atom transfer in batch and continuous flow. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30861204 DOI: 10.1002/Chem.201806092  0.406
2019 Dewanji A, Krach PE, Rueping M. The Dual Role of Benzophenone in Visible-Light/Nickel Photoredox-Catalyzed C-H Arylations: Hydrogen-Atom Transfer and Energy Transfer. Angewandte Chemie (International Ed. in English). 58: 3566-3570. PMID 30776185 DOI: 10.1002/Anie.201901327  0.738
2019 Akal AL, Karan R, Hohl A, Alam I, Vogler M, Grötzinger SW, Eppinger J, Rueping M. A polyextremophilic alcohol dehydrogenase from the Atlantis II Deep Red Sea brine pool. Febs Open Bio. 9: 194-205. PMID 30761247 DOI: 10.1002/2211-5463.12557  0.301
2019 Tretiakov M, Lebedev Y, Samantaray MK, Saidi A, Rueping M, Basset J. Metathesis of Functionalized Alkane: Understanding the Unsolved Story Catalysts. 9: 238. DOI: 10.3390/Catal9030238  0.379
2019 Blank L, Fagnoni M, Protti S, Rueping M. Visible Light-Promoted Formation of C–B and C–S Bonds under Metal- and Photocatalyst-Free Conditions Synthesis. 51: 1243-1252. DOI: 10.1055/S-0037-1611648  0.413
2019 Fabry DC, Heddrich S, Sugiono E, Liauw MA, Rueping M. Adaptive and automated system-optimization for heterogeneous flow-hydrogenation reactions Reaction Chemistry & Engineering. 4: 1486-1491. DOI: 10.1039/C9Re00032A  0.749
2019 Fabry DC, Zoller J, Rueping M. Semiconductors as heterogeneous visible light photoredox catalysts in combined dual metal catalyzed C–H functionalizations Organic Chemistry Frontiers. 6: 2635-2639. DOI: 10.1039/C9Qo00654K  0.796
2019 Kim HJ, Fabry DC, Mader S, Rueping M. Photoredox/rhodium catalysis in C–H activation for the synthesis of nitrogen containing heterocycles Organic Chemistry Frontiers. 6: 2319-2323. DOI: 10.1039/C9Qo00206E  0.79
2019 Szewczyk M, Magre M, Zubar V, Rueping M. Reduction of Cyclic and Linear Organic Carbonates Using a Readily Available Magnesium Catalyst Acs Catalysis. 9: 11634-11639. DOI: 10.1021/Acscatal.9B04086  0.771
2019 Ho YA, Paffenholz E, Kim HJ, Orgis B, Rueping M, Fabry DC. Catalytic Wacker‐type Oxidations Using Visible Light Photoredox Catalysis Chemcatchem. 11: 1889-1892. DOI: 10.1002/Cctc.201900271  0.726
2019 Kancherla R, Muralirajan K, Maity B, Zhu C, Krach PE, Cavallo L, Rueping M. Cover Picture: Oxidative Addition to Palladium(0) Made Easy through Photoexcited-State Metal Catalysis: Experiment and Computation (Angew. Chem. Int. Ed. 11/2019) Angewandte Chemie International Edition. 58: 3229-3229. DOI: 10.1002/Anie.201900572  0.719
2019 Kancherla R, Muralirajan K, Maity B, Zhu C, Krach PE, Cavallo L, Rueping M. Titelbild: Oxidative Addition to Palladium(0) Made Easy through Photoexcited-State Metal Catalysis: Experiment and Computation (Angew. Chem. 11/2019) Angewandte Chemie. 131: 3263-3263. DOI: 10.1002/Ange.201900572  0.72
2018 Borghs JC, Azofra LM, Biberger T, Linnenberg O, Cavallo L, Rueping M, El-Sepelgy O. Manganese-Catalyzed Multicomponent Synthesis of Pyrroles through Acceptorless Dehydrogenation Hydrogen Autotransfer Catalysis: Experiment and Computation. Chemsuschem. PMID 30589227 DOI: 10.1002/Cssc.201802416  0.796
2018 Borghs JC, Lebedev Y, Rueping M, El-Sepelgy O. Sustainable Manganese-Catalyzed Solvent-Free Synthesis of Pyrroles from 1,4-Diols and Primary Amines. Organic Letters. PMID 30582820 DOI: 10.1021/Acs.Orglett.8B03506  0.804
2018 Kancherla R, Muralirajan K, Maity B, Zhu C, Krach PE, Cavallo L, Rueping M. Oxidative Addition to Palladium(0) Made Easy through Photoexcited-State Metal Catalysis: Experiment and Computation. Angewandte Chemie (International Ed. in English). PMID 30520235 DOI: 10.1002/Anie.201811439  0.787
2018 Jang YK, Krückel T, Rueping M, El-Sepelgy O. Sustainable Alkylation of Unactivated Esters and Amides with Alcohols Enabled by Manganese Catalysis. Organic Letters. PMID 30507205 DOI: 10.1021/Acs.Orglett.8B03184  0.777
2018 Sklyaruk J, Borghs J, El-Sepelgy O, Rueping M. Catalytic C1-Alkylation with Methanol and Isotope Labelled Methanol. Angewandte Chemie (International Ed. in English). PMID 30457690 DOI: 10.1002/Anie.201810885  0.781
2018 Muralirajan K, Kancherla R, Rueping M. Dehydrogenative Aromatization and Sulfonylation of Pyrrolidines: Orthogonal Reactivity in Photoredox Catalysis. Angewandte Chemie (International Ed. in English). PMID 30307106 DOI: 10.1002/Anie.201808427  0.782
2018 El-Sepelgy O, Matador E, Brzozowska A, Rueping M. C-Alkylation of Secondary Alcohols by Primary Alcohols through Manganese-Catalyzed Double Hydrogen Autotransfer. Chemsuschem. PMID 30239145 DOI: 10.1002/Cssc.201801660  0.761
2018 Ho YA, Leiendecker M, Liu X, Wang C, Alandini N, Rueping M. Nickel-Catalyzed Csp-Csp Bond Formation via C-F Bond Activation. Organic Letters. PMID 30168331 DOI: 10.1021/Acs.Orglett.8B02351  0.814
2018 Rueping M. Hydrogenation of CO2-Derived Carbonates and Polycarbonates to Methanol and Diols via Metal Ligand Cooperative Manganese Catalysis. Angewandte Chemie (International Ed. in English). PMID 30102010 DOI: 10.1002/Anie.201805630  0.355
2018 Huang L, Rueping M. Direct Cross-Coupling of Allylic C(sp )-H Bonds with Aryl- and Vinylbromides by Combined Nickel and Visible-Light Catalysis. Angewandte Chemie (International Ed. in English). PMID 30011106 DOI: 10.1002/Anie.201805118  0.437
2018 Jia J, Ho YA, Bülow RF, Rueping M. Brønsted base assisted photoredox catalysis: Proton coupled electron transfer for remote C-C bond formations via amidyl radicals. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29939456 DOI: 10.1002/Chem.201802907  0.451
2018 Guo L, Rueping M. Transition-Metal-Catalyzed Decarbonylative Coupling Reactions: Concepts, Classifications, and Applications. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29757465 DOI: 10.1002/Chem.201704670  0.415
2018 Liu X, Hsiao CC, Guo L, Rueping M. Cross-Coupling of Amides with Alkylboranes via Nickel-Catalyzed C-N Bond Cleavage. Organic Letters. PMID 29741905 DOI: 10.1021/Acs.Orglett.8B01021  0.464
2018 Wang C, Maity B, Cavallo L, Rueping M. Manganese Catalyzed Regioselective C-H Alkylation: Experiment and Computation. Organic Letters. PMID 29738250 DOI: 10.1021/Acs.Orglett.8B01179  0.607
2018 Liao HH, Hsiao CC, Atodiresei I, Rueping M. Multiple Hydrogen-Bond Activation in Asymmetric Brønsted Acid Catalysis. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29722908 DOI: 10.1002/Chem.201800677  0.473
2018 Guo L, Rueping M. Decarbonylative Cross-Couplings: Nickel Catalyzed Functional Group Interconversion Strategies for the Construction of Complex Organic Molecules. Accounts of Chemical Research. PMID 29652129 DOI: 10.1021/Acs.Accounts.8B00023  0.51
2018 Chatupheeraphat A, Liao HH, Srimontree W, Guo L, Minenkov Y, Poater A, Cavallo L, Rueping M. Ligand-Controlled Chemoselective C(acyl)-O bond vs. C(aryl)-C bond Activation of Aromatic Esters in Nickel Catalyzed C(sp2)-C(sp3) Cross-Couplings. Journal of the American Chemical Society. PMID 29461813 DOI: 10.1021/Jacs.7B12865  0.458
2018 El-Sepelgy O, Brzozowska A, Sklyaruk J, Jang YK, Zubar V, Rueping M. Cooperative Metal-Ligand Catalyzed Intramolecular Hydroamination and Hydroalkoxylation of Allenes Using a Stable Iron Catalyst. Organic Letters. PMID 29345946 DOI: 10.1021/Acs.Orglett.7B03828  0.787
2018 Lee SC, Liao HH, Chatupheeraphat A, Rueping M. Nickel-Catalyzed C-S Bond Formation via Decarbonylative Thioetherification of Esters, Amides and Intramolecular Recombination Fragment Coupling of Thioesters. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29334411 DOI: 10.1002/Chem.201705842  0.452
2018 Yue H, Zhu C, Rueping M. Catalytic Ester to Stannane Functional Group Interconversion via Decarbonylative Cross-Coupling of Methyl Esters. Organic Letters. PMID 29297229 DOI: 10.1021/Acs.Orglett.7B03669  0.426
2018 Cai Y, Tang Y, Fan L, Lefebvre Q, Hou H, Rueping M. Heterogeneous Visible-Light Photoredox Catalysis with Graphitic Carbon Nitride for α-Aminoalkyl Radical Additions, Allylations, and Heteroarylations Acs Catalysis. 8: 9471-9476. DOI: 10.1021/Acscatal.8B02937  0.664
2018 Kalsi D, Dutta S, Barsu N, Rueping M, Sundararaju B. Room-Temperature C–H Bond Functionalization by Merging Cobalt and Photoredox Catalysis Acs Catalysis. 8: 8115-8120. DOI: 10.1021/Acscatal.8B02118  0.418
2018 Borrmann R, Palchyk V, Pich A, Rueping M. Reversible Switching and Recycling of Adaptable Organic Microgel Catalysts (Microgelzymes) for Asymmetric Organocatalytic Desymmetrization Acs Catalysis. 8: 7991-7996. DOI: 10.1021/Acscatal.8B01408  0.346
2018 Brzozowska A, Azofra LM, Zubar V, Atodiresei I, Cavallo L, Rueping M, El-Sepelgy O. Highly Chemo- and Stereoselective Transfer Semihydrogenation of Alkynes Catalyzed by a Stable, Well-Defined Manganese(II) Complex Acs Catalysis. 8: 4103-4109. DOI: 10.1021/Acscatal.8B00983  0.775
2018 Pluta R, Krach PE, Cavallo L, Falivene L, Rueping M. Metal-Free Catalytic Asymmetric Fluorination of Keto Esters Using a Combination of Hydrogen Fluoride (HF) and Oxidant: Experiment and Computation Acs Catalysis. 8: 2582-2588. DOI: 10.1021/Acscatal.7B03118  0.466
2018 Poscharny K, Fabry D, Heddrich S, Sugiono E, Liauw M, Rueping M. Machine assisted reaction optimization: A self-optimizing reactor system for continuous-flow photochemical reactions Tetrahedron. 74: 3171-3175. DOI: 10.1016/J.Tet.2018.04.019  0.751
2018 Hou H, Zhu S, Atodiresei I, Rueping M. Asymmetric Organocatalysis and Photoredox Catalysis for the α-Functionalization of Tetrahydroisoquinolines European Journal of Organic Chemistry. 2018: 1277-1280. DOI: 10.1002/Ejoc.201800117  0.707
2018 Guo L, Rueping M. Frontispiece: Transition-Metal-Catalyzed Decarbonylative Coupling Reactions: Concepts, Classifications, and Applications Chemistry - a European Journal. 24. DOI: 10.1002/Chem.201883162  0.375
2018 Wang C, Rueping M. Rhenium- and Manganese-Catalyzed Selective Alkenylation of Indoles Chemcatchem. 10: 2681-2685. DOI: 10.1002/Cctc.201800553  0.349
2017 Yue H, Zhu C, Rueping M. Cross-Coupling of Sodium Sulfinates with Aryl, Heteroaryl and Vinyl Halides by Nickel/photoredox dual catalysis. Angewandte Chemie (International Ed. in English). PMID 29211330 DOI: 10.1002/Anie.201711104  0.457
2017 Rueping M. Experimental and computational study of an unexpected iron catalyzed carboetherfication by cooperative metal and ligand substrate interaction and proton shuttle. Angewandte Chemie (International Ed. in English). PMID 28949059 DOI: 10.1002/Anie.201708240  0.338
2017 Chatupheeraphat A, Liao HH, Lee SC, Rueping M. Nickel-Catalyzed C-CN Bond Formation via Decarbonylative Cyanation of Esters, Amides, and Intramolecular Recombination Fragment Coupling of Acyl Cyanides. Organic Letters. PMID 28782964 DOI: 10.1021/Acs.Orglett.7B01905  0.483
2017 Parmar D, Sugiono E, Raja S, Rueping M. Addition and Correction to Complete Field Guide to Asymmetric BINOL-Phosphate Derived Brønsted Acid and Metal Catalysis: History and Classification by Mode of Activation; Brønsted Acidity, Hydrogen Bonding, Ion Pairing, and Metal Phosphates. Chemical Reviews. PMID 28737901 DOI: 10.1021/Acs.Chemrev.7B00197  0.335
2017 Rueping M. Synthesis of Amidines from Amides using a Nickel Catalyzed Decarbonylative Amination via CO Extrusion Intramolecular Recombination Fragment Coupling. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28695654 DOI: 10.1002/Chem.201702867  0.455
2017 Rueping M. Manganese catalyzed C-H functionalizations involving an unexpected heteroaryl-shift. Angewandte Chemie (International Ed. in English). PMID 28646490 DOI: 10.1002/anie.201704682  0.442
2017 Srimontree W, Chatupheeraphat A, Liao HH, Rueping M. Amide to Alkyne Interconversion via a Nickel/Copper-Catalyzed Deamidative Cross-Coupling of Aryl and Alkenyl Amides. Organic Letters. PMID 28581761 DOI: 10.1021/Acs.Orglett.7B01194  0.438
2017 Yue H, Guo L, Lee SC, Liu X, Rueping M. Selective Reductive Removal of Ester and Amide Groups from Arenes and Heteroarenes through Nickel-Catalyzed C-O and C-N Bond Activation. Angewandte Chemie (International Ed. in English). 56: 3972-3976. PMID 28321978 DOI: 10.1002/Anie.201612624  0.451
2017 El-Sepelgy O, Alandini N, Rueping M. Corrigendum: Merging Iron Catalysis and Biocatalysis-Iron Carbonyl Complexes as Efficient Hydrogen Autotransfer Catalysts in Dynamic Kinetic Resolutions. Angewandte Chemie (International Ed. in English). 56: 3129. PMID 28297194 DOI: 10.1002/anie.201700967  0.731
2017 Yue H, Guo L, Liao HH, Cai Y, Zhu C, Rueping M. Catalytic Ester and Amide to Amine Interconversion: Nickel-Catalyzed Decarbonylative Amination of Esters and Amides by C-O and C-C Bond Activation. Angewandte Chemie (International Ed. in English). PMID 28294473 DOI: 10.1002/Anie.201611819  0.734
2017 Yue H, Guo L, Liu X, Rueping M. Nickel-Catalyzed Synthesis of Primary Aryl and Heteroaryl Amines via C-O Bond Cleavage. Organic Letters. PMID 28287744 DOI: 10.1021/Acs.Orglett.7B00556  0.432
2017 Rueping M. Asymmetric Chemoenzymatic Reductive Acylation of Ketones Using a Combined Iron Catalyzed Hydrogenation-Racemization and Enzymatic Resolution Cascade. Chemsuschem. PMID 28244251 DOI: 10.1002/Cssc.201700169  0.422
2017 Rueping M, Lee S, Guo L, Yue H, Liao H. Nickel-Catalyzed Decarbonylative Silylation, Borylation, and Amination of Arylamides via a Deamidative Reaction Pathway Synlett. 28: 2594-2598. DOI: 10.1055/S-0036-1591495  0.473
2017 Fabry DC, Ho YA, Zapf R, Tremel W, Panthöfer M, Rueping M, Rehm TH. Blue light mediated C–H arylation of heteroarenes using TiO2 as an immobilized photocatalyst in a continuous-flow microreactor Green Chemistry. 19: 1911-1918. DOI: 10.1039/C7Gc00497D  0.723
2017 Liu X, Jia J, Rueping M. Nickel-Catalyzed C–O Bond-Cleaving Alkylation of Esters: Direct Replacement of the Ester Moiety by Functionalized Alkyl Chains Acs Catalysis. 7: 4491-4496. DOI: 10.1021/Acscatal.7B00941  0.447
2016 Rueping M. Asymmetric Synthesis of Optically Active Spirocyclic Indoline Scaffolds Applying an Enantioselective Reduction of 3H-Indoles. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27902876 DOI: 10.1002/Chem.201605450  0.483
2016 Guo L, Liu X, Baumann C, Rueping M. Nickel-Catalyzed Alkoxy-Alkyl Interconversion with Alkylborane Reagents through C-O Bond Activation of Aryl and Enol Ethers. Angewandte Chemie (International Ed. in English). 55: 15415-15419. PMID 27897421 DOI: 10.1002/Anie.201607646  0.427
2016 Cai Y, Tang Y, Atodiresei I, Rueping M. Catalytic Asymmetric Piancatelli Rearrangement: Brønsted Acid Catalyzed 4π Electrocyclization for the Synthesis of Multisubstituted Cyclopentenones. Angewandte Chemie (International Ed. in English). PMID 27723211 DOI: 10.1002/Anie.201608023  0.72
2016 Guo L, Rueping M. Functional Group Interconversion: Decarbonylative Borylation of Esters for the Synthesis of Organoboronates. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27717095 DOI: 10.1002/Chem.201604504  0.449
2016 El-Sepelgy O, Alandini N, Rueping M. Merging Iron Catalysis and Biocatalysis-Iron Carbonyl Complexes as Efficient Hydrogen Autotransfer Catalysts in Dynamic Kinetic Resolutions. Angewandte Chemie (International Ed. in English). PMID 27682185 DOI: 10.1002/Anie.201606197  0.763
2016 Rueping M. Decarboxylative Aminomethylation of Arylsulfonates. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27661773 DOI: 10.1002/Chem.201604452  0.436
2016 Guo L, Chatupheeraphat A, Rueping M. Decarbonylative Silylation of Esters by Combined Nickel and Copper Catalysis for the Synthesis of Arylsilanes and Heteroarylsilanes. Angewandte Chemie (International Ed. in English). PMID 27560460 DOI: 10.1002/Anie.201604696  0.465
2016 Fabry DC, Rueping M. Merging Visible Light Photoredox Catalysis with Metal Catalyzed C-H Activations: On the Role of Oxygen and Superoxide Ions as Oxidants. Accounts of Chemical Research. PMID 27556812 DOI: 10.1021/Acs.Accounts.6B00275  0.791
2016 Fava E, Nakajima M, Nguyen AL, Rueping M. Photoredox-Catalyzed Ketyl-Olefin Coupling for the Synthesis of Substituted Chromanols. The Journal of Organic Chemistry. PMID 27442851 DOI: 10.1021/Acs.Joc.6B01006  0.436
2016 Millet A, Lefebvre Q, Rueping M. Visible-Light Photoredox-Catalyzed Giese Reaction: Decarboxylative Addition of Amino Acid Derived α-Amino Radicals to Electron-Deficient Olefins. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27321136 DOI: 10.1002/Chem.201602257  0.403
2016 Fava E, Millet A, Nakajima M, Loescher S, Rueping M. Reductive Umpolung of Carbonyl Derivatives with Visible-Light Photoredox Catalysis: Direct Access to Vicinal Diamines and Amino Alcohols via α-Amino Radicals and Ketyl Radicals. Angewandte Chemie (International Ed. in English). PMID 27136443 DOI: 10.1002/Anie.201511235  0.376
2016 Liu X, Hsiao CC, Kalvet I, Leiendecker M, Guo L, Schoenebeck F, Rueping M. Lewis Acid Assisted Nickel-Catalyzed Cross-Coupling of Aryl Methyl Ethers by C-O Bond-Cleaving Alkylation: Prevention of Undesired β-Hydride Elimination. Angewandte Chemie (International Ed. in English). PMID 27062726 DOI: 10.1002/Anie.201510497  0.818
2016 Chatupheeraphat A, Liao HH, Mader S, Sako M, Sasai H, Atodiresei I, Rueping M. Asymmetric Brønsted Acid Catalyzed Substitution of Diaryl Methanols with Thiols and Alcohols for the Synthesis of Chiral Thioethers and Ethers. Angewandte Chemie (International Ed. in English). PMID 26952288 DOI: 10.1002/Anie.201511179  0.446
2016 Nikolaienko P, Rueping M. Trifluoromethylselenolation of Aryldiazonium Salts: A mild and Convenient Copper-Catalyzed Procedure for the Introduction of the SeCF3 Group. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26797773 DOI: 10.1002/Chem.201504601  0.408
2016 Lefebvre Q, Hoffmann N, Rueping M. Photoorganocatalysed and visible light photoredox catalysed trifluoromethylation of olefins and (hetero)aromatics in batch and continuous flow. Chemical Communications (Cambridge, England). PMID 26736069 DOI: 10.1039/C5Cc09881E  0.313
2016 Rueping M, Borrmann R, Koenigs R, Zoller J. Asymmetric Hydrogenation of Cyclic Imines and Enamines: Access to 1,5-Benzodiazepine Pharmacophores Synthesis. 49: 310-318. DOI: 10.1055/S-0036-1589401  0.69
2016 Fava E, Nakajima M, Tabak MB, Rueping M. Tin-free visible light photoredox catalysed cyclisation of enamides as a mild procedure for the synthesis of γ-lactams Green Chemistry. 18: 4531-4535. DOI: 10.1039/C6Gc01099G  0.362
2016 Fabry DC, Sugiono E, Rueping M. Online monitoring and analysis for autonomous continuous flow self-optimizing reactor systems Reaction Chemistry & Engineering. 1: 129-133. DOI: 10.1039/C5Re00038F  0.683
2016 Guo L, Hsiao C, Yue H, Liu X, Rueping M. Nickel-Catalyzed Csp2–Csp3 Cross-Coupling via C–O Bond Activation Acs Catalysis. 6: 4438-4442. DOI: 10.1021/Acscatal.6B00801  0.402
2016 Nikolaienko P, Yildiz T, Rueping M. Trifluoromethylthiolation of Unsymmetrical λ3-Iodane Derivatives: Additive-Free, Selective and Scalable Introduction of the SCF3 Group European Journal of Organic Chemistry. 2016: 1091-1094. DOI: 10.1002/Ejoc.201501623  0.447
2016 Guo L, Liu X, Baumann C, Rueping M. Nickel-katalysierter Alkoxy-Alkyl-Austausch mit Alkylboranen mittels C-O-Aktivierung von Aryl- und Enolethern Angewandte Chemie. 128: 15641-15645. DOI: 10.1002/Ange.201607646  0.331
2016 El-Sepelgy O, Alandini N, Rueping M. Kombinierte Eisen- und Biokatalyse - Eisencarbonylkomplexe als effiziente Wasserstoff-Autotransferkatalysatoren für die dynamische kinetische Racematspaltung Angewandte Chemie. 128: 13800-13803. DOI: 10.1002/Ange.201606197  0.704
2016 Chatupheeraphat A, Liao H, Mader S, Sako M, Sasai H, Atodiresei I, Rueping M. Asymmetrische Brønsted-Säure-katalysierte Substitution von Diarylmethanolen mit Thiolen und Alkoholen zur Synthese von chiralen Thioethern und Ethern Angewandte Chemie. 128: 4882-4887. DOI: 10.1002/Ange.201511179  0.345
2016 Liu X, Hsiao C, Kalvet I, Leiendecker M, Guo L, Schoenebeck F, Rueping M. Lewis-Säure-unterstützte metallkatalysierte Kreuzkupplung: Alkylierung von Arylmethylethern unter C-O-Bindungsspaltung ohne β-Hydrideliminierung Angewandte Chemie. 128: 6198-6203. DOI: 10.1002/Ange.201510497  0.772
2015 Liao HH, Chatupheeraphat A, Hsiao CC, Atodiresei I, Rueping M. Asymmetric Brønsted Acid Catalyzed Synthesis of Triarylmethanes-Construction of Communesin and Spiroindoline Scaffolds. Angewandte Chemie (International Ed. in English). PMID 26545412 DOI: 10.1002/Anie.201505981  0.446
2015 Takizawa S, Kishi K, Yoshida Y, Mader S, Arteaga FA, Lee S, Hoshino M, Rueping M, Fujita M, Sasai H. Phosphine-Catalyzed β,γ-Umpolung Domino Reaction of Allenic Esters: Facile Synthesis of Tetrahydrobenzofuranones Bearing a Chiral Tetrasubstituted Stereogenic Carbon Center. Angewandte Chemie (International Ed. in English). PMID 26537173 DOI: 10.1002/Anie.201508022  0.459
2015 Volla CM, Fava E, Atodiresei I, Rueping M. Dual metal and Lewis base catalysis approach for asymmetric synthesis of dihydroquinolines and the α-arylation of aldehydes via N-acyliminium ions. Chemical Communications (Cambridge, England). 51: 15788-91. PMID 26365533 DOI: 10.1039/C5Cc05209B  0.811
2015 Nakajima M, Fava E, Loescher S, Jiang Z, Rueping M. Photoredox-Catalyzed Reductive Coupling of Aldehydes, Ketones, and Imines with Visible Light. Angewandte Chemie (International Ed. in English). PMID 26082970 DOI: 10.1002/Anie.201501556  0.49
2015 Hsiao CC, Raja S, Liao HH, Atodiresei I, Rueping M. Ortho-quinone methides as reactive intermediates in asymmetric brønsted Acid catalyzed cycloadditions with unactivated alkenes by exclusive activation of the electrophile. Angewandte Chemie (International Ed. in English). 54: 5762-5. PMID 25784558 DOI: 10.1002/Anie.201409850  0.506
2015 Fabry DC, Ronge MA, Rueping M. Immobilization and continuous recycling of photoredox catalysts in ionic liquids for applications in batch reactions and flow systems: catalytic alkene isomerization by using visible light. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 5350-4. PMID 25694030 DOI: 10.1002/Chem.201406653  0.774
2015 Lefebvre Q, Pluta R, Rueping M. Copper catalyzed oxidative coupling reactions for trifluoromethylselenolations--synthesis of R-SeCF3 compounds using air stable tetramethylammonium trifluoromethylselenate. Chemical Communications (Cambridge, England). 51: 4394-7. PMID 25675984 DOI: 10.1039/C4Cc10212F  0.454
2015 Fabry DC, Ronge MA, Zoller J, Rueping M. C-H functionalization of phenols using combined ruthenium and photoredox catalysis: in situ generation of the oxidant. Angewandte Chemie (International Ed. in English). 54: 2801-5. PMID 25644740 DOI: 10.1002/Anie.201408891  0.817
2015 Parmar D, Henkel L, Dib J, Rueping M. Iron catalysed cross-couplings of azetidines - application to the formal synthesis of a pharmacologically active molecule. Chemical Communications (Cambridge, England). 51: 2111-3. PMID 25536275 DOI: 10.1039/C4Cc09337B  0.394
2015 Raja S, Nakajima M, Rueping M. Experimental and computational study of the catalytic asymmetric 4π-electrocyclization of N-heterocycles. Angewandte Chemie (International Ed. in English). 54: 2762-5. PMID 25533025 DOI: 10.1002/Anie.201408020  0.446
2015 Guo L, Leiendecker M, Hsiao CC, Baumann C, Rueping M. Nickel catalyzed dealkoxylative C(sp2)-C(sp3) cross coupling reactions--stereospecific synthesis of allylsilanes from enol ethers. Chemical Communications (Cambridge, England). 51: 1937-40. PMID 25532100 DOI: 10.1039/C4Cc08187K  0.831
2015 Leiendecker M, Chatupheeraphat A, Rueping M. Metal catalyzed cross-coupling of aryl and benzyl methyl sulfides: Nickel catalyzed Caryl-Csp3 and Csp3Csp3 bond formations Organic Chemistry Frontiers. 2: 350-353. DOI: 10.1039/C5Qo00001G  0.84
2015 Kim H, Sugiono E, Nagata Y, Wagner M, Bonn M, Rueping M, Hunger J. Role of Ion-Pairs in Brønsted Acid Catalysis Acs Catalysis. 5: 6630-6633. DOI: 10.1021/Acscatal.5B01694  0.402
2015 Zoller J, Fabry DC, Rueping M. Unexpected dual role of titanium dioxide in the visible light heterogeneous catalyzed C-H arylation of heteroarenes Acs Catalysis. 5: 3900-3904. DOI: 10.1021/Acscatal.5B00668  0.815
2015 Atodiresei I, Vila C, Rueping M. Asymmetric organocatalysis in continuous flow: Opportunities for impacting industrial catalysis Acs Catalysis. 5: 1972-1985. DOI: 10.1021/Acscatal.5B00002  0.548
2015 Nakajima M, Fava E, Loescher S, Jiang Z, Rueping M. Eine additivarme photoredoxkatalysierte reduktive Kupplung von Aldehyden, Ketonen und Iminen mit sichtbarem Licht Angewandte Chemie. 127: 8952-8956. DOI: 10.1002/Ange.201501556  0.342
2015 Fabry DC, Ronge MA, Zoller J, Rueping M. C-H-Funktionalisierung von Phenolen durch kombinierte Ruthenium- und Photoredoxkatalyse mit sichtbarem Licht: In-situ-Erzeugung des Oxidationsmittels Angewandte Chemie. 127: 2843-2847. DOI: 10.1002/Ange.201408891  0.775
2014 Pluta R, Rueping M. Selective and scalable synthesis of trifluoromethanesulfenamides and fluorinated unsymmetrical disulfides using a shelf-stable electrophilic SCF3 reagent. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 17315-8. PMID 25382258 DOI: 10.1002/Chem.201405654  0.445
2014 Pluta R, Rueping M. Selective and Scalable Synthesis of Trifluoromethanesulfenamides and Fluorinated Unsymmetrical Disulfides using a Shelf-Stable Electrophilic SCF3 Reagent. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 25376871 DOI: 10.1002/Chem.405654  0.335
2014 Hsiao CC, Liao HH, Rueping M. Enantio- and diastereoselective access to distant stereocenters embedded within tetrahydroxanthenes: utilizing ortho-quinone methides as reactive intermediates in asymmetric Brønsted acid catalysis. Angewandte Chemie (International Ed. in English). 53: 13258-63. PMID 25287936 DOI: 10.1002/Anie.201406587  0.479
2014 Zoller J, Fabry DC, Ronge MA, Rueping M. Synthesis of indoles using visible light: photoredox catalysis for palladium-catalyzed C-H activation. Angewandte Chemie (International Ed. in English). 53: 13264-8. PMID 25284332 DOI: 10.1002/Anie.201405478  0.826
2014 Parmar D, Rueping M. Mild and metal-free oxy- and amino-fluorination for the synthesis of fluorinated heterocycles. Chemical Communications (Cambridge, England). 50: 13928-31. PMID 25259871 DOI: 10.1039/C4Cc05027D  0.453
2014 Leiendecker M, Hsiao CC, Guo L, Alandini N, Rueping M. Metal-catalyzed dealkoxylative C(aryl)-C(sp3) cross-coupling-replacement of aromatic methoxy groups of aryl ethers by employing a functionalized nucleophile. Angewandte Chemie (International Ed. in English). 53: 12912-5. PMID 25250516 DOI: 10.1002/Anie.201402922  0.838
2014 Hong X, Küçük HB, Maji MS, Yang YF, Rueping M, Houk KN. Mechanism and selectivity of N-triflylphosphoramide catalyzed (3(+) + 2) cycloaddition between hydrazones and alkenes. Journal of the American Chemical Society. 136: 13769-80. PMID 25226575 DOI: 10.1021/Ja506660C  0.734
2014 Parmar D, Sugiono E, Raja S, Rueping M. Complete field guide to asymmetric BINOL-phosphate derived Brønsted acid and metal catalysis: history and classification by mode of activation; Brønsted acidity, hydrogen bonding, ion pairing, and metal phosphates. Chemical Reviews. 114: 9047-153. PMID 25203602 DOI: 10.1021/Cr5001496  0.332
2014 Uria U, Vila C, Lin MY, Rueping M. Gold-catalyzed asymmetric allylic substitution of free alcohols: an enantioselective approach to chiral chromans with quaternary stereocenters for the synthesis of vitamin E and analogues. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 13913-7. PMID 25201099 DOI: 10.1002/Chem.201403768  0.63
2014 Fabry DC, Zoller J, Raja S, Rueping M. Combining rhodium and photoredox catalysis for C-H functionalizations of arenes: oxidative Heck reactions with visible light. Angewandte Chemie (International Ed. in English). 53: 10228-31. PMID 25159225 DOI: 10.1002/Anie.201400560  0.823
2014 Nikolaienko P, Pluta R, Rueping M. Direct trifluoromethylthiolation of alcohols under mild reaction conditions: conversion of R-OH into R-SCF3. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 9867-70. PMID 25042061 DOI: 10.1002/Chem.201402679  0.333
2014 Vila C, Lau J, Rueping M. Visible-light photoredox catalyzed synthesis of pyrroloisoquinolines via organocatalytic oxidation/[3 + 2] cycloaddition/oxidative aromatization reaction cascade with Rose Bengal. Beilstein Journal of Organic Chemistry. 10: 1233-8. PMID 24991273 DOI: 10.3762/Bjoc.10.122  0.62
2014 Volla CM, Das A, Atodiresei I, Rueping M. Fluorine effects in organocatalysis - asymmetric Brønsted acid assisted Lewis base catalysis for the synthesis of trifluoromethylated heterocycles exploiting the negative hyperconjugation of the CF3-group. Chemical Communications (Cambridge, England). 50: 7889-92. PMID 24911934 DOI: 10.1039/C4Cc03229B  0.814
2014 Lefebvre Q, Fava E, Nikolaienko P, Rueping M. Hydrotrifluoromethylthiolation of α-diazo esters--synthesis of α-SCF3 substituted esters. Chemical Communications (Cambridge, England). 50: 6617-9. PMID 24823676 DOI: 10.1039/C4Cc02060J  0.303
2014 Hou H, Zhu S, Pan F, Rueping M. Visible-light photoredox-catalyzed synthesis of nitrones: unexpected rate acceleration by water in the synthesis of isoxazolidines. Organic Letters. 16: 2872-5. PMID 24810928 DOI: 10.1021/Ol500893G  0.758
2014 Nakajima M, Lefebvre Q, Rueping M. Visible light photoredox-catalysed intermolecular radical addition of α-halo amides to olefins. Chemical Communications (Cambridge, England). 50: 3619-22. PMID 24572999 DOI: 10.1039/C4Cc00753K  0.404
2014 Rueping M, Liu X, Bootwicha T, Pluta R, Merkens C. Catalytic enantioselective trifluoromethylthiolation of oxindoles using shelf-stable N-(trifluoromethylthio)phthalimide and a cinchona alkaloid catalyst. Chemical Communications (Cambridge, England). 50: 2508-11. PMID 24458251 DOI: 10.1039/C3Cc49877H  0.398
2014 Pluta R, Nikolaienko P, Rueping M. Direct catalytic trifluoromethylthiolation of boronic acids and alkynes employing electrophilic shelf-stable N-(trifluoromethylthio)phthalimide. Angewandte Chemie (International Ed. in English). 53: 1650-3. PMID 24449094 DOI: 10.1002/Anie.201307484  0.403
2014 Parmar D, Maji MS, Rueping M. Catalytic and asymmetric fluorolactonisations of carboxylic acids through anion phase transfer. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 83-6. PMID 24356866 DOI: 10.1002/Chem.201303385  0.733
2014 Volla CM, Atodiresei I, Rueping M. Catalytic C-C bond-forming multi-component cascade or domino reactions: pushing the boundaries of complexity in asymmetric organocatalysis. Chemical Reviews. 114: 2390-431. PMID 24304297 DOI: 10.1021/Cr400215U  0.807
2014 Rueping M, Dufour J, Bui L. Convergent catalysis: Asymmetric synthesis of dihydroquinolines using a combined metal catalysis and organocatalysis approach Acs Catalysis. 4: 1021-1025. DOI: 10.1021/Cs401176S  0.381
2014 Fabry DC, Sugiono E, Rueping M. Self-optimizing reactor systems: Algorithms, on-line analytics, setups, and strategies for accelerating continuous flow process optimization Israel Journal of Chemistry. 54: 341-350. DOI: 10.1002/Ijch.201300080  0.698
2014 Zoller J, Fabry DC, Ronge MA, Rueping M. Synthese von Indolen mithilfe von sichtbarem Licht: Photoredoxkatalyse für die Palladium-katalysierte C-H-Aktivierung Angewandte Chemie. 126: 13480-13484. DOI: 10.1002/Ange.201405478  0.784
2014 Leiendecker M, Hsiao C, Guo L, Alandini N, Rueping M. Metallkatalysierte desalkoxylierende CAr-C sp 3-Kreuzkupplung - Austausch aromatischer Methoxygruppen von Arylethern unter Verwendung eines funktionalisierten Nukleophils Angewandte Chemie. 126: 13126-13129. DOI: 10.1002/Ange.201402922  0.774
2014 Fabry DC, Zoller J, Raja S, Rueping M. Kombinierte Rhodium- und Photoredoxkatalyse in der C-H-Funktionalisierung von Arenen: oxidative Heck-Reaktionen mit sichtbarem Licht Angewandte Chemie. 126: 10392-10396. DOI: 10.1002/Ange.201400560  0.779
2013 Sugiono E, Rueping M. A combined continuous microflow photochemistry and asymmetric organocatalysis approach for the enantioselective synthesis of tetrahydroquinolines. Beilstein Journal of Organic Chemistry. 9: 2457-62. PMID 24367413 DOI: 10.3762/Bjoc.9.284  0.485
2013 Bootwicha T, Liu X, Pluta R, Atodiresei I, Rueping M. N-trifluoromethylthiophthalimide: a stable electrophilic SCF3 -reagent and its application in the catalytic asymmetric trifluoromethylsulfenylation. Angewandte Chemie (International Ed. in English). 52: 12856-9. PMID 24123914 DOI: 10.1002/Anie.201304957  0.428
2013 Rueping M, Tolstoluzhsky N, Nikolaienko P. Copper-catalyzed trifluoromethyl thiolation--mild and efficient synthesis of trifluoromethyl thioethers. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 14043-6. PMID 24108595 DOI: 10.1002/Chem.201302692  0.458
2013 Lefebvre Q, Jentsch M, Rueping M. Continuous flow photocyclization of stilbenes - scalable synthesis of functionalized phenanthrenes and helicenes. Beilstein Journal of Organic Chemistry. 9: 1883-90. PMID 24062857 DOI: 10.3762/Bjoc.9.221  0.326
2013 Kaupmees K, Tolstoluzhsky N, Raja S, Rueping M, Leito I. On the acidity and reactivity of highly effective chiral Brønsted acid catalysts: establishment of an acidity scale. Angewandte Chemie (International Ed. in English). 52: 11569-72. PMID 24039083 DOI: 10.1002/Anie.201303605  0.336
2013 Liao HH, Hsiao CC, Sugiono E, Rueping M. Shedding light on Brønsted acid catalysis--a photocyclization-reduction reaction for the asymmetric synthesis of tetrahydroquinolines from aminochalcones in batch and flow. Chemical Communications (Cambridge, England). 49: 7953-5. PMID 23903260 DOI: 10.1039/C3Cc43996H  0.452
2013 Das A, Volla CM, Atodiresei I, Bettray W, Rueping M. Asymmetric ion pair catalysis of 6π electrocyclizations: Brønsted acid catalyzed enantioselective synthesis of optically active 1,4-dihydropyridazines. Angewandte Chemie (International Ed. in English). 52: 8008-11. PMID 23788474 DOI: 10.1002/Anie.201301638  0.797
2013 Hsiao CC, Liao HH, Sugiono E, Atodiresei I, Rueping M. Shedding light on organocatalysis-light-assisted asymmetric ion-pair catalysis for the enantioselective hydrogenation of pyrylium ions. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 9775-9. PMID 23744744 DOI: 10.1002/Chem.201300766  0.368
2013 Rueping M, Vila C. Visible light photoredox-catalyzed multicomponent reactions. Organic Letters. 15: 2092-5. PMID 23586924 DOI: 10.1021/Ol400317V  0.662
2013 Zhu S, Das A, Bui L, Zhou H, Curran DP, Rueping M. Oxygen switch in visible-light photoredox catalysis: radical additions and cyclizations and unexpected C-C-bond cleavage reactions. Journal of the American Chemical Society. 135: 1823-9. PMID 23330701 DOI: 10.1021/Ja309580A  0.784
2013 Vila C, Rueping M. Visible-light mediated heterogeneous C-H functionalization: Oxidative multi-component reactions using a recyclable titanium dioxide (TiO2) catalyst Green Chemistry. 15: 2056-2059. DOI: 10.1039/C3Gc40587G  0.653
2013 Rueping M, Vila C, Bootwicha T. Continuous flow organocatalytic C-H functionalization and cross-dehydrogenative coupling reactions: Visible light organophotocatalysis for multicomponent reactions and C-C, C-P bond formations Acs Catalysis. 3: 1676-1680. DOI: 10.1021/Cs400350J  0.636
2012 Rueping M, Raja S. Asymmetric Brønsted acid-catalyzed aza-Diels-Alder reaction of cyclic C-acylimines with cyclopentadiene. Beilstein Journal of Organic Chemistry. 8: 1819-24. PMID 23209517 DOI: 10.3762/Bjoc.8.208  0.49
2012 Rueping M, Maji MS, Küçük HB, Atodiresei I. Asymmetric Brønsted acid catalyzed cycloadditions--efficient enantioselective synthesis of pyrazolidines, pyrazolines, and 1,3-diamines from N-acyl hyrazones and alkenes. Angewandte Chemie (International Ed. in English). 51: 12864-8. PMID 23161809 DOI: 10.1002/Anie.201205813  0.728
2012 Zhu S, Rueping M. Merging visible-light photoredox and Lewis acid catalysis for the functionalization and arylation of glycine derivatives and peptides. Chemical Communications (Cambridge, England). 48: 11960-2. PMID 23128983 DOI: 10.1039/C2Cc36995H  0.73
2012 Rueping M, Volla CM, Atodiresei I. Catalytic asymmetric addition of aldehydes to oxocarbenium ions: a dual catalytic system for the synthesis of chromenes. Organic Letters. 14: 4642-5. PMID 22913599 DOI: 10.1021/Ol302084Q  0.816
2012 Raja S, Ieawsuwan W, Korotkov V, Rueping M. Asymmetric Brønsted acid-catalyzed nazarov cyclization of acyclic α-alkoxy dienones. Chemistry, An Asian Journal. 7: 2361-6. PMID 22851505 DOI: 10.1002/Asia.201200391  0.485
2012 Rueping M, Merino E, Bolte M. Efficient proline and prolinol ether mediated 3-component synthesis of 3- and 3,4-substituted chromenone derivatives. Organic & Biomolecular Chemistry. 10: 6201-10. PMID 22585353 DOI: 10.1039/C2Ob25443C  0.466
2012 Rueping M, Bootwicha T, Kambutong S, Sugiono E. Asymmetric calcium catalysis: highly enantioselective carbonyl-ene and Friedel-Crafts reactions for the synthesis of quaternary α-hydroxy esters bearing a trifluoromethyl group. Chemistry, An Asian Journal. 7: 1195-8. PMID 22438311 DOI: 10.1002/Asia.201200063  0.424
2012 Rueping M, Koenigs RM, Poscharny K, Fabry DC, Leonori D, Vila C. Dual catalysis: combination of photocatalytic aerobic oxidation and metal catalyzed alkynylation reactions--C-C bond formation using visible light. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 5170-4. PMID 22431393 DOI: 10.1002/Chem.201200050  0.839
2012 Rueping M, Bootwicha T, Sugiono E. Continuous-flow catalytic asymmetric hydrogenations: Reaction optimization using FTIR inline analysis. Beilstein Journal of Organic Chemistry. 8: 300-7. PMID 22423298 DOI: 10.3762/Bjoc.8.32  0.413
2012 Rueping M, Sundén H, Sugiono E. Unifying metal- and organocatalysis for asymmetric oxidative iminium activation: a relay catalytic system enabling the combined allylic oxidation of alcohols and prolinol ether catalyzed iminium reactions. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 3649-53. PMID 22374840 DOI: 10.1002/Chem.201102551  0.491
2012 Rueping M, Dufour J, Maji MS. Relay catalysis: combined metal catalyzed oxidation and asymmetric iminium catalysis for the synthesis of bi- and tricyclic chromenes. Chemical Communications (Cambridge, England). 48: 3406-8. PMID 22363938 DOI: 10.1039/C2Cc00129B  0.749
2012 Rueping M, Zoller J, Fabry DC, Poscharny K, Koenigs RM, Weirich TE, Mayer J. Light-mediated heterogeneous cross dehydrogenative coupling reactions: metal oxides as efficient, recyclable, photoredox catalysts in C-C bond-forming reactions. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 3478-81. PMID 22314870 DOI: 10.1002/Chem.201103242  0.835
2012 Rueping M, Vila C, Uria U. Direct catalytic azidation of allylic alcohols. Organic Letters. 14: 768-71. PMID 22256853 DOI: 10.1021/Ol203310H  0.641
2012 Rueping M, Sundén H, Hubener L, Sugiono E. Asymmetric oxidative Lewis base catalysis-unifying iminium and enamine organocatalysis with oxidations. Chemical Communications (Cambridge, England). 48: 2201-3. PMID 22252220 DOI: 10.1039/C2Cc16447G  0.369
2012 Rueping M, Nachtsheim BJ. Bismuth salts in catalytic alkylation reactions. Topics in Current Chemistry. 311: 115-41. PMID 21728137 DOI: 10.1007/128_2011_191  0.53
2012 Rueping M, Moreth SA, Bolte M. Asymmetric Brønsted acid-catalyzed intramolecular aza-michael reaction - Enantioselective synthesis of dihydroquinolinones Zeitschrift Fur Naturforschung - Section B Journal of Chemical Sciences. 67: 1021-1029. DOI: 10.5560/Znb.2012-0183  0.486
2012 Rueping M, Phapale VB. Effective synthesis of 2,5-disubstituted tetrahydrofurans from glycerol by catalytic alkylation of ketones Green Chemistry. 14: 55-57. DOI: 10.1039/C1Gc15764G  0.428
2012 Rueping M, Vila C, Szadkowska A, Koenigs RM, Fronert J. Photoredox catalysis as an efficient tool for the aerobic oxidation of amines and alcohols: Bioinspired demethylations and condensations Acs Catalysis. 2: 2810-2815. DOI: 10.1021/Cs300604K  0.602
2012 Rueping M, Rasappan R, Raja S. Asymmetric proline-catalyzed addition of aldehydes to 3H-indol-3-ones: Enantioselective synthesis of 2,3-dihydro-1H-indol-3-ones with quaternary stereogenic centers Helvetica Chimica Acta. 95: 2296-2303. DOI: 10.1002/Hlca.201200498  0.772
2012 Rueping M, Merino E, Sugiono E. Catalytic Asymmetric Synthesis of Chromene Derivatives by Iminium Ion Catalysis Chemcatchem. 4: 987-992. DOI: 10.1002/Cctc.201200151  0.461
2012 Rueping M, Maji MS, Küçük HB, Atodiresei I. Asymmetrische Brønsted-Säure-katalysierte Cycloadditionen - effiziente enantioselektive Synthese von Pyrazolidinen, Pyrazolinen und 1,3-Diaminen ausN-Acylhydrazonen und Alkenen Angewandte Chemie. 124: 13036-13040. DOI: 10.1002/Ange.201205813  0.672
2011 Rueping M, Bootwicha T, Baars H, Sugiono E. Continuous-flow hydration-condensation reaction: Synthesis of α,β-unsaturated ketones from alkynes and aldehydes by using a heterogeneous solid acid catalyst. Beilstein Journal of Organic Chemistry. 7: 1680-7. PMID 22238547 DOI: 10.3762/Bjoc.7.198  0.445
2011 Rueping M, Zhu S, Koenigs RM. Visible-light photoredox catalyzed oxidative Strecker reaction. Chemical Communications (Cambridge, England). 47: 12709-11. PMID 22041859 DOI: 10.1039/C1Cc15643H  0.78
2011 Rueping M, Leiendecker M, Das A, Poisson T, Bui L. Potassium tert-butoxide mediated Heck-type cyclization/isomerization-benzofurans from organocatalytic radical cross-coupling reactions. Chemical Communications (Cambridge, England). 47: 10629-31. PMID 21892507 DOI: 10.1039/C1Cc14297F  0.818
2011 Rueping M, Ieawsuwan W. Asymmetric Brønsted acid catalyzed carbonyl activation--organocatalytic domino electrocyclization-halogenation reaction. Chemical Communications (Cambridge, England). 47: 11450-2. PMID 21892501 DOI: 10.1039/C1Cc15289K  0.495
2011 Rueping M, Theissmann T, Stoeckel M, Antonchick AP. Direct enantioselective access to 4-substituted tetrahydroquinolines by catalytic asymmetric transfer hydrogenation of quinolines. Organic & Biomolecular Chemistry. 9: 6844-50. PMID 21837348 DOI: 10.1039/C1Ob05870C  0.684
2011 Rueping M, Leonori D, Poisson T. Visible light mediated azomethine ylide formation-photoredox catalyzed [3+2] cycloadditions. Chemical Communications (Cambridge, England). 47: 9615-7. PMID 21792444 DOI: 10.1039/C1Cc13660G  0.7
2011 Rueping M, Zhu S, Koenigs RM. Photoredox catalyzed C-P bond forming reactions-visible light mediated oxidative phosphonylations of amines. Chemical Communications (Cambridge, England). 47: 8679-81. PMID 21720622 DOI: 10.1039/C1Cc12907D  0.796
2011 Rueping M, Nachtsheim BJ, Ieawsuwan W, Atodiresei I. Modulating the acidity: highly acidic Brønsted acids in asymmetric catalysis. Angewandte Chemie (International Ed. in English). 50: 6706-20. PMID 21678531 DOI: 10.1002/Anie.201100169  0.427
2011 Fleischmann M, Drettwan D, Sugiono E, Rueping M, Gschwind RM. Brønsted acid catalysis: hydrogen bonding versus ion pairing in imine activation. Angewandte Chemie (International Ed. in English). 50: 6364-9. PMID 21638523 DOI: 10.1002/Anie.201101385  0.312
2011 Rueping M, Kuenkel A, Atodiresei I. Chiral Brønsted acids in enantioselective carbonyl activations--activation modes and applications. Chemical Society Reviews. 40: 4539-49. PMID 21614342 DOI: 10.1039/C1Cs15087A  0.418
2011 Rueping M, Haack K, Ieawsuwan W, Sundén H, Blanco M, Schoepke FR. Nature-inspired cascade catalysis: reaction control through substrate concentration--double vs. quadruple domino reactions. Chemical Communications (Cambridge, England). 47: 3828-30. PMID 21359352 DOI: 10.1039/C1Cc10245A  0.372
2011 Rueping M, Uria U, Lin MY, Atodiresei I. Chiral organic contact ion pairs in metal-free catalytic asymmetric allylic substitutions. Journal of the American Chemical Society. 133: 3732-5. PMID 21355548 DOI: 10.1021/Ja110213T  0.408
2011 Husmann R, Sugiono E, Mersmann S, Raabe G, Rueping M, Bolm C. Enantioselective organocatalytic synthesis of quaternary α-amino acids bearing a CF3 moiety. Organic Letters. 13: 1044-7. PMID 21348534 DOI: 10.1021/Ol103093R  0.461
2011 Rueping M, Tolstoluzhsky N. Copper catalyzed C-H functionalization for direct Mannich reactions. Organic Letters. 13: 1095-7. PMID 21288008 DOI: 10.1021/Ol103150G  0.491
2011 Rueping M, Vila C, Koenigs RM, Poscharny K, Fabry DC. Dual catalysis: combining photoredox and Lewis base catalysis for direct Mannich reactions. Chemical Communications (Cambridge, England). 47: 2360-2. PMID 21161098 DOI: 10.1039/C0Cc04539J  0.817
2011 Rueping M, Koenigs RM. Brønsted acid differentiated metal catalysis by kinetic discrimination. Chemical Communications (Cambridge, England). 47: 304-6. PMID 20717581 DOI: 10.1039/C0Cc02167A  0.399
2011 Rueping M, Hubener L. Enantioselective synthesis of quinolizidines and indolizidines via a catalytic asymmetric hydrogenation cascade Synlett. 1243-1246. DOI: 10.1055/S-0030-1259955  0.478
2011 Rueping M, Bootwicha T, Sugiono E. Chiral brønsted acids and their calcium salts in catalytic asymmetric mannich reactions of cyclic 1,3-diketones Synlett. 323-326. DOI: 10.1055/S-0030-1259318  0.433
2011 Rueping M, Volla CMR. Brønsted-acid catalyzed condensation-Michael reaction-Pictet- Spengler cyclization - Highly stereoselective synthesis of indoloquinolizidines Rsc Advances. 1: 79-82. DOI: 10.1039/C1Ra00305D  0.469
2011 Rueping M, Dufour J, Schoepke FR. Advances in catalytic metal-free reductions: From bio-inspired concepts to applications in the organocatalytic synthesis of pharmaceuticals and natural products Green Chemistry. 13: 1084-1105. DOI: 10.1039/C1Gc15027H  0.432
2011 Rueping M, Koenigs RM, Borrmann R, Zoller J, Weirich TE, Mayer J. Size-selective, stabilizer-free, hydrogenolytic synthesis of iridium nanoparticles supported on carbon nanotubes Chemistry of Materials. 23: 2008-2010. DOI: 10.1021/Cm1032578  0.589
2011 Rueping M, Nachtsheim BJ, Ieawsuwan W, Atodiresei I. Modulation der Acidität - hoch acide Brønsted-Säuren in der asymmetrischen Katalyse Angewandte Chemie. 123: 6838-6853. DOI: 10.1002/Ange.201100169  0.347
2011 Rueping M, Volla CMR, Bolte M, Raabe G. General and efficient organocatalytic synthesis of indoloquinolizidines, pyridoquinazolines and quinazolinones through a one-pot domino michael addition-cyclization-pictet-spengler or 1,2-amine addition reaction Advanced Synthesis and Catalysis. 353: 2853-2859. DOI: 10.1002/Adsc.201100258  0.459
2011 Rueping M, Raja S, Núñez A. Asymmetric Brønsted acid-catalyzed Friedel-Crafts reactions of indoles with cyclic imines - Efficient generation of nitrogen-substituted quaternary carbon centers Advanced Synthesis and Catalysis. 353: 563-568. DOI: 10.1002/Adsc.201000952  0.48
2010 Rueping M, Parra A, Uria U, Besselièvre F, Merino E. Catalytic asymmetric domino Michael addition-alkylation reaction: enantioselective synthesis of dihydrofurans. Organic Letters. 12: 5680-3. PMID 21090798 DOI: 10.1021/Ol102499R  0.499
2010 Rueping M, Parra A. Fast, efficient, mild, and metal-free synthesis of pyrroles by domino reactions in water. Organic Letters. 12: 5281-3. PMID 20979413 DOI: 10.1021/Ol102247N  0.427
2010 Rueping M, Nachtsheim BJ, Koenigs RM, Ieawsuwan W. Synthesis and structural aspects of N-triflylphosphoramides and their calcium salts--highly acidic and effective Brønsted acids. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 13116-26. PMID 20922721 DOI: 10.1002/Chem.201001438  0.35
2010 Rueping M, Brinkmann C, Antonchick AP, Atodiresei I. Asymmetric synthesis of indolines by catalytic enantioselective reduction of 3H-indoles. Organic Letters. 12: 4604-7. PMID 20857958 DOI: 10.1021/Ol1019234  0.686
2010 Rueping M, Koenigs RM, Atodiresei I. Unifying metal and Brønsted acid catalysis--concepts, mechanisms, and classifications. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 9350-65. PMID 20665582 DOI: 10.1002/Chem.201001140  0.414
2010 Rueping M, Nachtsheim BJ. A review of new developments in the Friedel-Crafts alkylation - From green chemistry to asymmetric catalysis. Beilstein Journal of Organic Chemistry. 6: 6. PMID 20485588 DOI: 10.3762/Bjoc.6.6  0.447
2010 Rueping M, Kuenkel A, Fröhlich R. Catalytic asymmetric domino Michael-Henry reaction: enantioselective access to bicycles with consecutive quaternary centers by using bifunctional catalysts. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 4173-6. PMID 20309980 DOI: 10.1002/Chem.201000237  0.472
2010 Rueping M, Lin MY. Catalytic asymmetric mannich-ketalization reaction: highly enantioselective synthesis of aminobenzopyrans. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 4169-72. PMID 20309979 DOI: 10.1002/Chem.201000203  0.496
2010 Rueping M, Tato F, Schoepke FR. The first general, efficient and highly enantioselective reduction of quinoxalines and quinoxalinones. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 2688-91. PMID 20140920 DOI: 10.1002/Chem.200902907  0.443
2010 Rueping M, Nachtsheim BJ, Sugiono E. Direct catalytic benzylation of hydroxycoumarin - Efficient synthesis of warfarin derivatives and analogues Synlett. 1549-1553. DOI: 10.1055/S-0029-1219936  0.509
2010 Rueping M, Sugiono E, Schoepke FR. Thieme chemistry journal awardees - Where are they now? Asymmetric br?nsted acid catalyzed transfer hydrogenations Synlett. 852-865. DOI: 10.1055/S-0029-1219528  0.454
2010 Rueping M, Nachtsheim BJ. Asymmetric brønsted acid catalyzed nucleophilic addition to in situ generated chiral N-acyliminium ions Synlett. 119-122. DOI: 10.1055/S-0029-1218539  0.426
2010 Rueping M, Theissmann T. Asymmetric Brønsted acid catalysis in aqueous solution Chemical Science. 1: 473-476. DOI: 10.1039/C0Sc00206B  0.372
2010 Rueping M, Stoeckel M, Sugiono E, Theissmann T. Asymmetric metal-free synthesis of fluoroquinolones by organocatalytic hydrogenation Tetrahedron. 66: 6565-6568. DOI: 10.1016/J.Tet.2010.04.091  0.401
2010 Rueping M, Merino E, Koenigs RM. First highly enantioselective synthesis of benzodiazepinones by catalytic hydrogenation Advanced Synthesis and Catalysis. 352: 2629-2634. DOI: 10.1002/Adsc.201000547  0.464
2010 Rueping M, Bootwicha T, Sugiono E. Efficient and general continuous-flow hydroarylation and hydroalkylation of styrenes Advanced Synthesis and Catalysis. 352: 2961-2965. DOI: 10.1002/Adsc.201000538  0.32
2010 Rueping M, Sugiono E, Steck A, Theissmann T. Synthesis and application of polymer-supported chiral Brønsted acid organocatalysts Advanced Synthesis and Catalysis. 352: 281-287. DOI: 10.1002/Adsc.200900746  0.454
2009 Kadyrov R, Koenigs RM, Brinkmann C, Voigtlaender D, Rueping M. Efficient enantioselective synthesis of optically active Diols by asymmetric hydrogenation with modular chiral metal catalysts. Angewandte Chemie (International Ed. in English). 48: 7556-9. PMID 19739156 DOI: 10.1002/Anie.200902835  0.43
2009 Rueping M, Kuenkel A, Tato F, Bats JW. Asymmetric organocatalytic domino Michael/aldol reactions: enantioselective synthesis of chiral cycloheptanones, tetrahydrochromenones, and polyfunctionalized bicyclo[3.2.1]octanes. Angewandte Chemie (International Ed. in English). 48: 3699-702. PMID 19378300 DOI: 10.1002/Anie.200900754  0.467
2009 Rueping M, Antonchick AP, Sugiono E, Grenader K. Asymmetric Brønsted acid catalysis: catalytic enantioselective synthesis of highly biologically active dihydroquinazolinones. Angewandte Chemie (International Ed. in English). 48: 908-10. PMID 19101974 DOI: 10.1002/Anie.200804770  0.668
2009 Kadyrov R, Koenigs R, Brinkmann C, Voigtlaender D, Rueping M. Effiziente enantioselektive Synthese von optisch aktiven Diolen durch asymmetrische Hydrierung mittels modular aufgebauter chiraler Metallkatalysatoren Angewandte Chemie. 121: 7693-7696. DOI: 10.1002/Ange.200902835  0.342
2009 Rueping M, Kuenkel A, Tato F, Bats J. Eine asymmetrische organokatalytische Domino-Michael-Aldol- Reaktion: enantioselektiver Zugang zu chiralen Cycloheptanonen, Tetrahydrochromenonen und polyfunktionalisierten Bicyclo[3.2.1]octanen Angewandte Chemie. 121: 3754-3757. DOI: 10.1002/Ange.200900754  0.404
2009 Rueping M, Antonchick A, Sugiono E, Grenader K. Asymmetrische Brønsted-Säure-Katalyse: katalytische enantioselektive Synthese von hochaktiven Dihydrochinazolinon-Wirkstoffen Angewandte Chemie. 121: 925-927. DOI: 10.1002/Ange.200804770  0.602
2009 Rueping M, Ieawsuwan W. A catalytic asymmetric electrocyclization-protonation reaction Advanced Synthesis and Catalysis. 351: 78-84. DOI: 10.1002/Adsc.200800623  0.474
2008 Rueping M, Antonchick AP. Catalytic asymmetric aminoallylation of aldehydes: a catalytic enantioselective aza-Cope rearrangement. Angewandte Chemie (International Ed. in English). 47: 10090-3. PMID 19025749 DOI: 10.1002/Anie.200803610  0.684
2008 Rueping M, Theissmann T, Kuenkel A, Koenigs RM. Highly enantioselective organocatalytic carbonyl-ene reaction with strongly acidic, chiral Brønsted acids as efficient catalysts. Angewandte Chemie (International Ed. in English). 47: 6798-801. PMID 18655079 DOI: 10.1002/Anie.200802139  0.459
2008 Rueping M, Sugiono E, Merino E. Asymmetric organocatalysis: an efficient enantioselective access to benzopyranes and chromenes. Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 6329-32. PMID 18576457 DOI: 10.1002/Chem.200800836  0.373
2008 Rueping M, Antonchick AP. A highly enantioselective Brønsted acid catalyzed reaction cascade. Angewandte Chemie (International Ed. in English). 47: 5836-8. PMID 18576441 DOI: 10.1002/Anie.200801435  0.678
2008 Rueping M, Antonchick AP. Brønsted-acid-catalyzed activation of nitroalkanes: a direct enantioselective aza-Henry reaction. Organic Letters. 10: 1731-4. PMID 18393508 DOI: 10.1021/Ol8003589  0.675
2008 Rueping M, Sugiono E, Merino E. Asymmetric iminium ion catalysis: an efficient enantioselective synthesis of pyranonaphthoquinones and beta-lapachones. Angewandte Chemie (International Ed. in English). 47: 3046-9. PMID 18327864 DOI: 10.1002/Anie.200705110  0.316
2008 Rueping M, Nachtsheim BJ, Moreth SA, Bolte M. Asymmetric Brønsted acid catalysis: enantioselective nucleophilic substitutions and 1,4-additions. Angewandte Chemie (International Ed. in English). 47: 593-6. PMID 18095369 DOI: 10.1002/Anie.200703668  0.413
2008 Rueping M, Antonchick AP. ChemInform Abstract: Broensted-Acid-Catalyzed Activation of Nitroalkanes: A Direct Enantioselective Aza-Henry Reaction. Cheminform. 39. DOI: 10.1002/chin.200837075  0.642
2008 Rueping M, Antonchick A. Katalytische asymmetrische Aminoallylierung von Aldehyden - eine katalytische enantioselektive Aza-Cope-Umlagerung Angewandte Chemie. 120: 10244-10247. DOI: 10.1002/Ange.200803610  0.555
2008 Rueping M, Antonchick A. Eine hoch enantioselektive Brønsted‐Säure‐katalysierte Reaktionskaskade Angewandte Chemie. 120: 5920-5922. DOI: 10.1002/Ange.200801435  0.551
2008 Rueping M, Nachtsheim B, Moreth S, Bolte M. Asymmetrische Brønsted-Säure-Katalyse: enantioselektive nucleophile Substitutionen und 1,4-Additionen Angewandte Chemie. 120: 603-606. DOI: 10.1002/Ange.200703668  0.418
2008 Rueping M, Merino E, Sugiono E. Enantioselective organocatalytic reactions of 4-hydroxy-coumarin and 4-hydroxypyrone with α,β-unsaturated aldehydes - An efficient Michael addition-acetalization cascade to chromenones, quinolinones and pyranones Advanced Synthesis and Catalysis. 350: 2127-2131. DOI: 10.1002/Adsc.200800340  0.44
2008 Rueping M, Theissmann T, Raja S, Bats JW. Asymmetric counterion pair catalysis: An enantioselective Brønsted acid-catalyzed protonation Advanced Synthesis and Catalysis. 350: 1001-1006. DOI: 10.1002/Adsc.200800020  0.476
2007 Rueping M, Sugiono E. New developments in enantioselective Brønsted acid catalysis: chiral ion pair catalysis and beyond. Ernst Schering Foundation Symposium Proceedings. 207-53. PMID 18642527  0.378
2007 Rueping M, Antonchick AP, Brinkmann C. Dual catalysis: a combined enantioselective Brønsted acid and metal-catalyzed reaction--metal catalysis with chiral counterions. Angewandte Chemie (International Ed. in English). 46: 6903-6. PMID 17694520 DOI: 10.1002/Anie.200702439  0.657
2007 Rueping M, Antonchick AP. Organocatalytic enantioselective reduction of pyridines. Angewandte Chemie (International Ed. in English). 46: 4562-5. PMID 17492817 DOI: 10.1002/Anie.200701158  0.657
2007 Rueping M, Sugiono E, Theissmann T, Kuenkel A, Köckritz A, Pews-Davtyan A, Nemati N, Beller M. An enantioselective chiral Brønsted acid catalyzed imino-azaenamine reaction. Organic Letters. 9: 1065-8. PMID 17305351 DOI: 10.1021/Ol063112P  0.464
2007 Rueping M, Ieawsuwan W, Antonchick AP, Nachtsheim BJ. Chiral Brønsted acids in the catalytic asymmetric Nazarov cyclization--the first enantioselective organocatalytic electrocyclic reaction. Angewandte Chemie (International Ed. in English). 46: 2097-100. PMID 17278163 DOI: 10.1002/Anie.200604809  0.694
2007 Rueping M, Nachtsheim BJ, Kuenkel A. Efficient metal-catalyzed direct benzylation and allylic alkylation of 2,4-pentanediones. Organic Letters. 9: 825-8. PMID 17263542 DOI: 10.1021/Ol063048B  0.498
2007 Rueping M, Sugiono E, Schoepke FR. Development of the first Brønsted acid assisted enantioselective Brønsted acid catalyzed direct Mannich reaction Synlett. 1441-1445. DOI: 10.1055/S-2007-980369  0.439
2007 Rueping M, Nachtsheim BJ, Kuenkel A. An efficient metal-catalyzed hydroalkylation Synlett. 1391-1394. DOI: 10.1055/S-2007-980363  0.46
2007 Rueping M, Ieawsuwan W, Antonchick A, Nachtsheim B. Brønsted Acid Catalyzed Asymmetric Nazarov Cyclization Synfacts. 2007: 0432-0432. DOI: 10.1055/s-2007-968354  0.606
2007 Rueping M, Ieawsuwan W. A manganese-catalyzed cross-coupling reaction Synlett. 247-250. DOI: 10.1055/S-2007-968013  0.463
2007 Rueping M. Enantioselective Organocatalytic Cascade Reactions Cheminform. 38. DOI: 10.1002/chin.200719236  0.314
2007 Rueping M, Antonchick A, Brinkmann C. Duale Katalyse: eine kombinierte enantioselektive Brønsted-Säure- und metallkatalysierte Reaktion – Metallkatalyse mit chiralem Gegenion Angewandte Chemie. 119: 7027-7030. DOI: 10.1002/Ange.200702439  0.539
2007 Rueping M, Antonchick A. Organokatalytische enantioselektive Reduktion von Pyridinen Angewandte Chemie. 119: 4646-4649. DOI: 10.1002/Ange.200701158  0.527
2007 Rueping M, Ieawsuwan W, Antonchick A, Nachtsheim B. Chirale Brønsted-Säuren in der katalytischen asymmetrischen Nazarov-Reaktion – die erste enantioselektive organokatalytische elektrocyclische Reaktion Angewandte Chemie. 119: 2143-2146. DOI: 10.1002/Ange.200604809  0.589
2007 Rueping M, Sugiono E, Moreth SA. Metal-free, enantioselective strecker reactions catalyzed by chiral BINOL and TADDOL catalysts Advanced Synthesis and Catalysis. 349: 759-764. DOI: 10.1002/Adsc.200600405  0.511
2007 Rueping M, Sugiono E, Azap C, Theissmann T, Antonchick AP, Nawaz Khan S, Cho NJ, Kim HS. Imine Reduction and Reductive Amination Regio- and Stereo-Controlled Oxidations and Reductions. 5: 161-181. DOI: 10.1002/9780470090244.ch4  0.58
2006 Rueping M, Azap C. Cooperative coexistence: effective interplay of two Brønsted acids in the asymmetric synthesis of isoquinuclidines. Angewandte Chemie (International Ed. in English). 45: 7832-5. PMID 17080478 DOI: 10.1002/Anie.200603199  0.354
2006 Rueping M, Antonchick AP, Theissmann T. Remarkably low catalyst loading in Brønsted acid catalyzed transfer hydrogenations: enantioselective reduction of benzoxazines, benzothiazines, and benzoxazinones. Angewandte Chemie (International Ed. in English). 45: 6751-5. PMID 16986184 DOI: 10.1002/Anie.200601832  0.644
2006 Rueping M, Nachtsheim BJ, Scheidt T. Efficient metal-catalyzed hydroarylation of styrenes. Organic Letters. 8: 3717-9. PMID 16898800 DOI: 10.1021/Ol0612962  0.458
2006 Rueping M, Antonchick AP, Theissmann T. A highly enantioselective Brønsted acid catalyzed cascade reaction: organocatalytic transfer hydrogenation of quinolines and their application in the synthesis of alkaloids. Angewandte Chemie (International Ed. in English). 45: 3683-6. PMID 16639754 DOI: 10.1002/Anie.200600191  0.692
2006 Rueping M, Sugiono E, Azap C. A highly enantioselective Brønsted acid catalyst for the Strecker reaction. Angewandte Chemie (International Ed. in English). 45: 2617-9. PMID 16544358 DOI: 10.1002/Anie.200504344  0.457
2006 Rueping M. Aldol reactions within the RNA world. Angewandte Chemie (International Ed. in English). 45: 1838-40. PMID 16521102 DOI: 10.1002/Anie.200504053  0.301
2006 Rueping M, Antonchick A, Theissmann T. Highly Enantioselective Organocatalytic Transfer Hydrogenation of Quinolines Synfacts. 2006: 0731-0731. DOI: 10.1055/s-2006-941911  0.563
2006 Rueping M, Sugiono E, Azap C. Asymmetric Strecker Reaction Catalyzed by a Brønsted Acid Synfacts. 2006: 0613-0613. DOI: 10.1055/s-2006-941788  0.324
2006 Rueping M, Theissmann T, Antonchick AP. Metal-free Brønsted acid catalyzed transfer hydrogenation - New organocatalytic reduction of quinolines Synlett. 1071-1074. DOI: 10.1055/S-2006-939706  0.681
2006 Hüttenhain SH, Schmidt MU, Schoepke FR, Rueping M. Chiral induction from solvents-lactic acid esters in the asymmetric hydroboration of ketones Tetrahedron. 62: 12420-12423. DOI: 10.1016/J.Tet.2006.09.111  0.4
2006 Rueping M, Azap C. Kooperative Koexistenz: effizientes Zusammenspiel zweier Brønsted-Säuren in der asymmetrischen Synthese von Isochinuclidinen Angewandte Chemie. 118: 7996-7999. DOI: 10.1002/Ange.200603199  0.319
2006 Rueping M, Antonchick AP, Theissmann T. Geringste Katalysatormengen in der Brønsted-Säure-katalysierten Transferhydrierung: enantioselektive Reduktion von Benzoxazinen, Benzthiazinen und Benzoxazinonen Angewandte Chemie. 118: 6903-6907. DOI: 10.1002/Ange.200601832  0.555
2006 Rueping M, Antonchick AP, Theissmann T. Eine hoch enantioselektive Brønsted-Säure-katalysierte Kaskadenreaktion: organokatalytische Transferhydrierung von Chinolinen und deren Anwendung in der Synthese von Alkaloiden Angewandte Chemie. 118: 3765-3768. DOI: 10.1002/Ange.200600191  0.588
2006 Rueping M, Nachtsheim BJ, Ieawsuwan W. An effective bismuth-catalyzed benzylation of arenes and heteroarenes Advanced Synthesis and Catalysis. 348: 1033-1037. DOI: 10.1002/Adsc.200606068  0.468
2005 Rueping M, Sugiono E, Azap C, Theissmann T, Bolte M. Enantioselective Brønsted acid catalyzed transfer hydrogenation: organocatalytic reduction of imines. Organic Letters. 7: 3781-3. PMID 16092874 DOI: 10.1021/Ol0515964  0.456
2005 Rueping M, Azap C, Sugiono E, Theissmann T. Brønsted acid catalysis: Organocatalytic hydrogenation of imines Synlett. 2367-2369. DOI: 10.1055/S-2005-872251  0.389
2005 Seebach D, Mathad RI, Kimmerlin T, Mahajan YR, Bindschädler P, Rueping M, Jaun B, Hilty C, Etezady-Esfarjani T. NMR-solution structures in methanol of an α-heptapeptide, of a β3/β2-nonapeptide, and of an all-β3-icosapeptide carrying the 20 proteinogenic side chains Helvetica Chimica Acta. 88: 1969-1982. DOI: 10.1002/Hlca.200590151  0.387
2004 Wiegand H, Wirz B, Schweitzer A, Gross G, Perez MI, Andres H, Kimmerlin T, Rueping M, Seebach D. Pharmacokinetic investigation of a 14C-labelled beta 3/alpha tetrapeptide in rats. Chemistry & Biodiversity. 1: 1812-28. PMID 17191818 DOI: 10.1002/Cbdv.200490136  0.387
2004 Rueping M, Mahajan YR, Jaun B, Seebach D. Design, synthesis and structural investigations of a beta-peptide forming a 314-helix stabilized by electrostatic interactions. Chemistry (Weinheim An Der Bergstrasse, Germany). 10: 1607-15. PMID 15054747 DOI: 10.1002/Chem.200305571  0.38
2004 Rueping M, Albert M, Seebach D. On the structure of PHB (=Poly[(R)-3-hydroxybutanoic acid]) in phospholipid bilayers: Preparation of trifluoromethyl-labeled oligo[(R)-3-hydroxybutanoic acid] derivatives Helvetica Chimica Acta. 87: 2473-2486. DOI: 10.1002/Hlca.200490222  0.39
2003 Peter C, Rueping M, Wörner HJ, Jaun B, Seebach D, van Gunsteren WF. Molecular dynamics simulations of small peptides: can one derive conformational preferences from ROESY spectra? Chemistry (Weinheim An Der Bergstrasse, Germany). 9: 5838-49. PMID 14673855 DOI: 10.1002/Chem.200305147  0.403
2003 Evans DA, Seidel D, Rueping M, Lam HW, Shaw JT, Downey CW. A new copper acetate-bis(oxazoline)-catalyzed, enantioselective Henry reaction. Journal of the American Chemical Society. 125: 12692-3. PMID 14558801 DOI: 10.1021/Ja0373871  0.826
2003 Gademann K, Häne A, Rueping M, Jaun B, Seebach D. The fourth helical secondary structure of beta-peptides: the (P)-28-helix of a beta-hexapeptide consisting of (2R,3S)-3-amino-2-hydroxy acid residues. Angewandte Chemie (International Ed. in English). 42: 1534-7. PMID 12698493 DOI: 10.1002/Anie.200250290  0.577
2003 Nunn C, Rueping M, Langenegger D, Schuepbach E, Kimmerlin T, Micuch P, Hurth K, Seebach D, Hoyer D. Beta(2)/beta(3)-di- and alpha/beta(3)-tetrapeptide derivatives as potent agonists at somatostatin sst(4) receptors. Naunyn-Schmiedeberg's Archives of Pharmacology. 367: 95-103. PMID 12595949 DOI: 10.1007/S00210-002-0673-4  0.351
2003 Gessier F, Noti C, Rueping M, Seebach D. Synthesis and CD spectra of fluoro- and hydroxy-substituted β-peptides Helvetica Chimica Acta. 86: 1862-1870. DOI: 10.1002/Hlca.200390150  0.424
2003 Gademann K, Häne A, Rueping M, Jaun B, Seebach D. Die vierte helicale Sekundärstruktur von β-Peptiden: (P)-28-Helix eines β-Hexapeptids aus (2R,3S)-3-Amino-2-hydroxycarbonsäure-Einheiten Angewandte Chemie. 115: 1573-1575. DOI: 10.1002/Ange.200250290  0.575
2003 Rueping M, Schreiber JV, Lelais G, Jaun B, Seebach D. Mixed β2/β3-Hexapeptides and β2/β3-Nonapeptides Folding to (P)-Helices with Alternating Twelve- and Ten-Membered Hydrogen-Bonded Rings. Cheminform. 34: no-no. DOI: 10.1002/1522-2675(200209)85:9<2577::Aid-Hlca2577>3.0.Co;2-D  0.392
2002 Seebach D, Mahajan YR, Senthilkumar R, Rueping M, Jaun B. Beta-depsipeptides--the effect of a missing and a weakened hydrogen bond on the stability of the beta-peptidic 3(14)-helix. Chemical Communications (Cambridge, England). 1598-9. PMID 12170800 DOI: 10.1039/B204187C  0.383
2002 Rueping M, Mahajan Y, Sauer M, Seebach D. Cellular uptake studies with beta-peptides. Chembiochem : a European Journal of Chemical Biology. 3: 257-9. PMID 11921409 DOI: 10.1002/1439-7633(20020301)3:2/3<257::Aid-Cbic257>3.0.Co;2-S  0.34
2002 Seebach D, Brenner M, Rueping M, Jaun B. Gamma2-, gamma3-, and gamma(2,3,4)-amino acids, coupling to gamma-hexapeptides: CD spectra, NMR solution and X-ray crystal structures of gamma-peptides. Chemistry (Weinheim An Der Bergstrasse, Germany). 8: 573-84. PMID 11855705 DOI: 10.1002/1521-3765(20020201)8:3<573::Aid-Chem573>3.0.Co;2-H  0.424
2002 Seebach D, Sifferlen T, Bierbaum DJ, Rueping M, Jaun B, Schweizer B, Schaefer J, Mehta AK, O'Connor RD, Meier BH, Ernst M, Glättli A. Isotopically labelled and unlabelled β-peptides with geminal dimethyl substitution in 2-position of each residue: Synthesis and NMR investigation in solution and in the solid state Helvetica Chimica Acta. 85: 2877-2917. DOI: 10.1002/1522-2675(200209)85:9<2877::Aid-Hlca2877>3.0.Co;2-W  0.45
2002 Etezady-Esfarjani T, Hilty C, Wüthrich K, Rueping M, Schreiber J, Seebach D. NMR-structural investigations of a β3-dodecapeptide with proteinogenic side chains in methanol and in aqueous solutions Helvetica Chimica Acta. 85: 1197-1209. DOI: 10.1002/1522-2675(200205)85:5<1197::Aid-Hlca1197>3.0.Co;2-E  0.381
2001 Arvidsson PI, Rueping M, Seebach D. Design, machine synthesis, and NMR-solution structure of a β-heptapeptide forming a salt-bridge stabilised 314-helix in methanol and in water Chemical Communications. 649-650. DOI: 10.1039/B101085I  0.605
2001 Seebach D, Brenner M, Rueping M, Schweizer B, Jaun B. Preparation and determination of X-ray-crystal and NMR-solution structures of γ2,3,4-peptides Chemical Communications. 207-208. DOI: 10.1039/B008377L  0.401
2001 Rueping M, Dietrich A, Buschmann V, Fritz MG, Sauer M, Seebach D. On the structure of poly(3-hydroxybutanoic acid) in solution and in phospholipid bilayers. Circular dichroism and fluorescence spectroscopy with oligo(3-hydroxybutanoic acid) derivatives Macromolecules. 34: 7042-7048. DOI: 10.1021/Ma010520U  0.397
2001 Seebach D, Rueping M, Arvidsson PI, Kimmerlin T, Micuch P, Noti C, Langenegger D, Hoyer D. Linear, peptidase-resistant β 2/β 3-Di- and α/β 3-tetrapeptide derivatives with nanomolar affinities to a human somatostatin receptor Helvetica Chimica Acta. 84: 3503-3510. DOI: 10.1002/1522-2675(20011114)84:11<3503::Aid-Hlca3503>3.0.Co;2-A  0.585
2001 Waser P, Rueping M, Seebach D, Duchardt E, Schwalbe H. On the solution structure of PHB: Preparation and NMR analysis of isotopically labeled oligo[(R)-3-hydroxybutanoic acids] (OHBs) Helvetica Chimica Acta. 84: 1821-1845. DOI: 10.1002/1522-2675(20010613)84:6<1821::Aid-Hlca1821>3.0.Co;2-C  0.436
2001 Arvidsson PI, Rueping M, Seebach D. Design, machine synthesis, and NMR-solution structure of a β-heptapeptide forming a salt-bridge stabilised 314-helix in methanol and in water Chemical Communications. 649-650.  0.498
2000 Rueping M, Jaun B, Seebach D. NMR structure in methanol of a β-hexapeptide with a disulfide clamp Chemical Communications. 2267-2268. DOI: 10.1039/B007503P  0.4
2000 Seebach D, Jacobi A, Rueping M, Gademann K, Ernst M, Jaun B. Synthesis of β-hexa- and β-heptapeptides containing novel β 2,3-amino acids with two serine or two cysteine side chains - CD- and NMR-spectroscopic evidence for 3 14-helical secondary structures in water Helvetica Chimica Acta. 83: 2115-2140. DOI: 10.1002/1522-2675(20000906)83:9<2115::Aid-Hlca2115>3.0.Co;2-E  0.587
1999 Sifferlen T, Rueping M, Gademann K, Jaun B, Seebach D. β-thiopeptides: Synthesis, NMR solution structure, CD spectra and photochemistry Helvetica Chimica Acta. 82: 2067-2093. DOI: 10.1002/(Sici)1522-2675(19991215)82:12<2067::Aid-Hlca2067>3.0.Co;2-5  0.594
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