P. Srinivas
Indian Institute of Chemical Technology
29 Papers
322 Citations
P. Srinivas is an academic researcher from Indian Institute of Chemical Technology. The author has contributed to research in topics: Catalysis & Palladium. The author has an hindex of 13, co-authored 29 publications.
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Papers
Asymmetric hydrosilylation of ketones catalyzed by magnetically recoverable and reusable copper ferrite nanoparticles.
TL;DR: In this paper, magnetically recoverable and reusable copper ferrite nanoparticles were used for asymmetric hydrosilylation of several ketones, and up to 99% enantiometric excess was obtained at room temperature using polymethylhydrosiloxane as the stoichiometric reducing agent.
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Trifunctional N,N,O-terdentate amido/pyridyl carboxylate ligated Pd(II) complexes for Heck and Suzuki reactions.
TL;DR: Trifunctional N,N,O-terdentate amido/pyridyl carboxylate Pd(II) complexes were highly active and stable phosphine-free catalysts for Heck and room-temperature Suzuki reactions with high turnover numbers up to ca.
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N4‐Tetradentate Dicarboxyamidate/Dipyridyl Palladium Complexes as Robust Catalysts for the Heck Reaction of Deactivated Aryl Chlorides
P. Srinivas,Pravin R. Likhar,H. Maheswaran,Balasubramanian Sridhar,Krishnan Ravikumar,Mannepalli Lakshmi Kantam +5 more
TL;DR: The concept of using an anionic carboxyamide as an ancillary ligand for palladium demonstrated here provides a new opportunity for the development of phosphine-free transition-metal catalysis.
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Asymmetric Hydrosilylation of Ketones Catalyzed by Magnetically Recoverable and Reusable Copper Ferrite Nanoparticles.
TL;DR: In this article, magnetically recoverable and reusable copper ferrite nanoparticles were used for asymmetric hydrosilylation of several ketones, and up to 99% enantiometric excess was obtained at room temperature using polymethylhydrosiloxane as the stoichiometric reducing agent.
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Fluorapatite‐Supported Palladium Catalyst for Suzuki and Heck Coupling Reactions of Haloarenes
TL;DR: A fluorapatite-supported palladium catalyst (PdFAP) was synthesized by treatment of the basic species fluoride ion into apatite in situ by co-precipitation with bis(benzonitrile)palladium(II) chloride in acetone as mentioned in this paper.
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