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Anant R. Kapdi
Researcher at Institute of Chemical Technology
Publications - 135
Citations - 5981
Anant R. Kapdi is an academic researcher from Institute of Chemical Technology. The author has contributed to research in topics: Catalysis & Palladium. The author has an hindex of 26, co-authored 120 publications receiving 5298 citations. Previous affiliations of Anant R. Kapdi include University of Göttingen & Indian Institute of Technology Kharagpur.
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Journal ArticleDOI
1,3,5-Triaza-7-phosphaadamantane (PTA) Derived Caged Phosphines for Palladium-Catalyzed Selective Functionalization of Nucleosides and Heteroarenes
TL;DR: The research group has been working extensively for the past several years in the development of 1,3,5‐triaza‐7‐phosphaadamantane‐based caged ligands and in this personal note they have summarized these applications pertaining to the modification of biologically useful nucleosides and heteroarenes.
Journal ArticleDOI
Extended fluorescent uridine analogues: synthesis, photophysical properties and selective interaction with BSA protein
Ajaykumar V. Ardhapure,Vijay Gayakhe,Shatrughn Bhilare,Anant R. Kapdi,Subhendu Sekhar Bag,Yogesh S. Sanghvi,Krishna Chaitanya Gunturu +6 more
TL;DR: The improvement in fluorescence properties of 2′-deoxyuridine was brought about by the introduction of (hetero)aromatic moieties at the C–5 position of uridine directly or via alkenyl/phenyl/styryl linkers to create a library of biologically useful fluorescent nucleosides.
Book ChapterDOI
Palladacycles as Potential Anticancer Agents
TL;DR: According to the WHO, this disease was responsible for an estimated 9.6 million deaths in 2018 alone, indicating that the cancer burden is still a daunting concern and a challenge for public health care systems worldwide.
Journal ArticleDOI
Organophotoredox-Catalyzed C–H Alkylation of Imidazoheterocycles with Malonates: Total Synthesis of Zolpidem
TL;DR: In this article, an organophotoredox-catalyzed C-H functionalization of imidazo[1,2-a]pyridines and related heterocycles with bromomalonates under mild conditions is reported, providing excellent yields of the products at room temperature.
Book ChapterDOI
Stille Cross-Coupling Reaction: Early Years to the Current State of the Art
TL;DR: In this article, the authors highlight the usefulness of the catalytic process in the synthesis of modified nucleosides and highlight the use of catalytic catalysts in the process of cross-coupling reactions.