S
Suvajit Koley
Researcher at Banaras Hindu University
Publications - 59
Citations - 992
Suvajit Koley is an academic researcher from Banaras Hindu University. The author has contributed to research in topics: Catalysis & Annulation. The author has an hindex of 14, co-authored 58 publications receiving 771 citations. Previous affiliations of Suvajit Koley include University of Kansas & Sanjay Gandhi Post Graduate Institute of Medical Sciences.
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Advances of azide-alkyne cycloaddition-click chemistry over the recent decade
TL;DR: This review describes the general features and applications of CuAAC in organic synthesis (CuAAC-OS), highlighting the suitability of this kind of reaction for peptides, nucleotides, small molecules, supramolecular structures, and polymers among others.
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Progress in 1,3-dipolar cycloadditions in the recent decade: an update to strategic development towards the arsenal of organic synthesis
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Recent Advances in Transition Metal-Catalyzed Functionalization of gem-Difluoroalkenes.
Suvajit Koley,Ryan A. Altman +1 more
TL;DR: Recent (since 2017) transition metal-catalyzed transformations of these specialized alkenes are reviewed and general reactivity patterns of these reactions are summarized.
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Cross-Dehydrogenating Coupling of Aldehydes with Amines/R-OTBS Ethers by Visible-Light Photoredox Catalysis: Synthesis of Amides, Esters, and Ureas.
TL;DR: A straightforward synthesis of amides, ureas, and esters is reported by visible-light cross-dehydrogenating coupling of aldehydes and amines/R-OTBS ethers by photoredox catalysis.
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Connecting remote C-H bond functionalization and decarboxylative coupling using simple amines.
Francisco de Azambuja,Francisco de Azambuja,Ming-Hsiu Yang,Ming-Hsiu Yang,Taisiia Feoktistova,Manikandan Selvaraju,Alexander C. Brueckner,Markas A. Grove,Suvajit Koley,Paul Ha-Yeon Cheong,Ryan A. Altman +10 more
TL;DR: A catalytic para -selective alkylation reaction connects C–H functionalization and decarboxylative coupling strategies using simple bases to trap a previously hidden intermediate and exploits an ‘inverted sequence’ that forms the C–C bond prior to C-H bond cleavage and provides a new entry into C–h functionalization reactions.