R
Ranadeep Talukdar
Researcher at Sanjay Gandhi Post Graduate Institute of Medical Sciences
Publications - 24
Citations - 322
Ranadeep Talukdar is an academic researcher from Sanjay Gandhi Post Graduate Institute of Medical Sciences. The author has contributed to research in topics: Ring (chemistry) & Catalysis. The author has an hindex of 7, co-authored 23 publications receiving 262 citations. Previous affiliations of Ranadeep Talukdar include Indian Institute of Technology Kanpur & Indian Institute of Technology Kharagpur.
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Diastereoselective synthesis of functionalized tetrahydrocarbazoles via a domino-ring opening-cyclization of donor-acceptor cyclopropanes with substituted 2-vinylindoles.
TL;DR: A new domino synthetic approach for the synthesis of highly functionalized tetrahydrocarbazoles via DROC of various functionalized DA-cyclopropanes with 2-indolylnitroethylene and indole-substituted alkylidene malonate is described.
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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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Domino‐Ring Opening‐Cyclization (DROC) of Donor‐Acceptor (DA) Cyclopropanes
TL;DR: In this article, a new concept called "domino-ring opening cyclization" (DROC) is introduced, where both the reactive centres of the DA cyclopropane participate in the bond formation, with a suitable reagent bearing both nucleophilic and electrophilic terminals in a domino fashion.
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A Route to Highly Functionalized β-Enaminoesters via a Domino Ring-Opening Cyclization/Decarboxylative Tautomerization Sequence of Donor–Acceptor Cyclopropanes with Substituted Malononitriles
TL;DR: An unprecedented and domino synthetic strategy for the synthesis of highly functionalized carbocyclic β-enaminoesters bearing an all-carbon quaternary center via Yb(OTf)3-catalyzed ring-opening cyclization/decarboxylative tautomerization of donor-acceptor cyclopropanes with 2-alkyl malononitriles in excellent yields is described.
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An efficient synthetic route to carbocyclic enaminonitriles via Lewis acid catalysed domino-ring-opening-cyclisation (DROC) of donor-acceptor cyclopropanes with malononitrile.
TL;DR: A highly efficient strategy for the synthesis of functionalised carbocyclic enaminonitriles in excellent yields has been described.