B
Beneesh P. Babu
Researcher at National Institute of Technology, Karnataka
Publications - 33
Citations - 1215
Beneesh P. Babu is an academic researcher from National Institute of Technology, Karnataka. The author has contributed to research in topics: Catalysis & Nucleophile. The author has an hindex of 11, co-authored 31 publications receiving 1083 citations. Previous affiliations of Beneesh P. Babu include Council of Scientific and Industrial Research & National Institute for Interdisciplinary Science and Technology.
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Journal ArticleDOI
Recent advances in carbon–carbon bond-forming reactions involving homoenolates generated by NHC catalysis
TL;DR: The versatility of NHC-bound homoenolate is illustrated by its annulation with various carbonyl compounds leading to gamma-butyrolactones, spiro-gamma- butyrolactsones, and delta-lactones.
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Carbon-nitrogen bond-forming reactions of dialkyl azodicarboxylate: a promising synthetic strategy.
TL;DR: In this article, the potential utility of azodicarboxylates in various carbon-nitrogen bond-forming reactions is summarized, including electrophilic amination and pericyclic reactions.
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Stereoselective synthesis of spirocyclopentanones via N-heterocyclic carbene-catalyzed reactions of enals and dienones.
TL;DR: Homoenolates generated from enals by nucleophilic heterocyclic carbene (NHC) catalysis undergo a conjugate addition/cyclization sequence with cyclic dienones, culminating in the efficient synthesis of spirocyclopentanones.
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Nucleophilic heterocyclic carbene catalyzed annulation of enals to chalcones in methanol: A stereoselective synthesis of highly functionalized cyclopentanes
Vijay Nair,Beneesh P. Babu,Sreekumar Vellalath,Vimal Varghese,Anabha E. Raveendran,Eringathodi Suresh +5 more
TL;DR: Construction of four contiguous stereocenters in a stereoselective manner is noteworthy inhomoenolates generated from enals by nucleophilic heterocyclic carbene (NHC) catalysis.
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Novel nucleophilic heterocyclic carbene mediated stereoselective conjugate addition of enals to nitrostyrenes via homoenolate.
TL;DR: A stereoselective Michael addition of homoenolate, generated from enals by nucleophilic heterocyclic carbene (NHC) catalysis, to beta-nitrostyrenes is reported for the first time.