Auxofuran, a Novel Metabolite That Stimulates the Growth of Fly Agaric, Is Produced by the Mycorrhiza Helper Bacterium Streptomyces Strain AcH 505 J Riedlinger, SD Schrey, MT Tarkka, R Hampp, M Kapur, HP Fiedler Applied and environmental microbiology 72 (5), 3550-3557, 2006 | 219 | 2006 |
Ruthenium-catalyzed, site-selective C–H allylation of indoles with allyl alcohols as coupling partners GS Kumar, M Kapur Organic letters 18 (5), 1112-1115, 2016 | 128 | 2016 |
Ruthenium-catalyzed heteroatom-directed regioselective C–H arylation of indoles using a removable tether VK Tiwari, N Kamal, M Kapur Organic letters 17 (7), 1766-1769, 2015 | 107 | 2015 |
Transition‐Metal‐Catalyzed Site‐Selective C− H Halogenation Reactions R Das, M Kapur Asian Journal of Organic Chemistry 7 (8), 1524-1541, 2018 | 98 | 2018 |
Amides as weak coordinating groups in proximal C–H bond activation R Das, GS Kumar, M Kapur European Journal of Organic Chemistry 2017 (37), 5439-5459, 2017 | 94 | 2017 |
Transition metal-catalyzed C–H functionalizations of indoles P Kumar, PJ Nagtilak, M Kapur New Journal of Chemistry 45 (31), 13692-13746, 2021 | 83 | 2021 |
Palladium (II)-Catalyzed, Heteroatom-Directed, Regioselective C–H Nitration of Anilines Using Pyrimidine as a Removable Directing Group GG Pawar, A Brahmanandan, M Kapur Organic letters 18 (3), 448-451, 2016 | 83 | 2016 |
Palladium-Catalyzed, ortho-Selective C–H Halogenation of Benzyl Nitriles, Aryl Weinreb Amides, and Anilides R Das, M Kapur The Journal of organic chemistry 82 (2), 1114-1126, 2017 | 79 | 2017 |
Traceless directing-group strategy in the Ru-catalyzed, formal [3+ 3] annulation of anilines with allyl alcohols: a one-pot, domino approach for the synthesis of quinolines GS Kumar, P Kumar, M Kapur Organic letters 19 (10), 2494-2497, 2017 | 69 | 2017 |
A new access to polyhydroxy piperidines of the azasugar class: synthesis and glycosidase inhibition studies G Pandey, M Kapur, MI Khan, SM Gaikwad Organic & biomolecular chemistry 1 (19), 3321-3326, 2003 | 65 | 2003 |
Design and Development of a Common Synthetic Strategy for a Variety of 1-N-Iminosugars G Pandey, M Kapur Organic Letters 4 (22), 3883-3886, 2002 | 64 | 2002 |
A general strategy towards the synthesis of 1-N-iminosugar type glycosidase inhibitors: demonstration by the synthesis of d-as well as l-glucose type iminosugars (isofagomines) G Pandey, M Kapur Tetrahedron Letters 41 (45), 8821-8824, 2000 | 62 | 2000 |
Catalyst-controlled positional-selectivity in C–H functionalizations VK Tiwari, M Kapur Organic & Biomolecular Chemistry 17 (5), 1007-1026, 2019 | 59 | 2019 |
Transition‐Metal‐Catalyzed C− H Functionalization Reactions of π‐Deficient Heterocycles R Das, M Kapur Asian Journal of Organic Chemistry 7 (7), 1217-1235, 2018 | 59 | 2018 |
Concise strategy to the core structure of the macrolide queenslandon AS Khartulyari, M Kapur, ME Maier Organic letters 8 (25), 5833-5836, 2006 | 58 | 2006 |
Ruthenium-catalyzed C–H functionalization of benzoic acids with allyl alcohols: A controlled reactivity switch between C–H alkenylation and C–H alkylation pathways GS Kumar, T Chand, D Singh, M Kapur Organic letters 20 (16), 4934-4937, 2018 | 56 | 2018 |
Catalyst control in positional-selective C–H alkenylation of isoxazoles and a ruthenium-mediated assembly of trisubstituted pyrroles P Kumar, M Kapur Organic letters 21 (7), 2134-2138, 2019 | 55 | 2019 |
Temperature induced morphological transitions from native to unfolded aggregated states of human serum albumin NK Das, N Ghosh, AP Kale, R Mondal, U Anand, S Ghosh, VK Tiwari, ... The journal of physical chemistry B 118 (26), 7267-7276, 2014 | 55 | 2014 |
Dehydrogenative Heck reaction (Fujiwara–Moritani reaction) of unactivated olefins with simple dihydropyrans under aprotic conditions GG Pawar, G Singh, VK Tiwari, M Kapur Advanced Synthesis & Catalysis 355 (11‐12), 2185-2190, 2013 | 49 | 2013 |
Transition‐Metal‐Catalyzed C−H Bond Functionalization of Arenes/Heteroarenes via Tandem C−H Activation and Subsequent Carbene Migratory Insertion Strategy N Jha, NP Khot, M Kapur The Chemical Record 21 (12), 4088-4122, 2021 | 48 | 2021 |