S
Subbarayappa Adimurthy
Researcher at Central Salt and Marine Chemicals Research Institute
Publications - 155
Citations - 3906
Subbarayappa Adimurthy is an academic researcher from Central Salt and Marine Chemicals Research Institute. The author has contributed to research in topics: Catalysis & Bromide. The author has an hindex of 31, co-authored 151 publications receiving 3362 citations. Previous affiliations of Subbarayappa Adimurthy include Indian National Association & Council of Scientific and Industrial Research.
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Comparative study of the vicinal functionalization of olefins with 2:1 bromide/bromate and iodide/iodate reagents
TL;DR: In this paper, a comparative evaluation was made on the syntheses of vicinal halohydrins, halo methyl ethers, and halo acetates from olefins using 2:1 Br−/BrO3− and I−/IO3− reagents.
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C3 Sulfenylation of N-Heteroarenes in Water under Catalyst-Free Conditions
TL;DR: A catalyst-free selective C−H sulfenylation of imidazo[1,2-a]pyridines using sulfonothioates as odorless source of thioarylated reagent in an aqueous medium with broad functional group tolerance is described.
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Visible-light-promoted selective C-H amination of heteroarenes with heteroaromatic amines under metal-free conditions.
TL;DR: The regioselective C-H amination of quinoline amides and imidazopyridines under transition-metal-free conditions at room temperature with a high degree of functional group tolerance is reported.
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Synthesis of Indolizines through Oxidative Linkage of C–C and C–N Bonds from 2-Pyridylacetates
TL;DR: This protocol is compatible with a broad range of functional groups, and it has been also successfully extended to unsaturated ketones, bringing about the regioselective formation of benzoyl-substituted indolizines through Michael addition followed by C-N bond formation, which are difficult to prepare by previous methods in a single step.
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Facile one-pot synthesis of α-bromoketones from olefins using bromide/bromate couple as a nonhazardous brominating agent
TL;DR: In this article, a method for the preparation of α-bromoketones from olefins using bromide/bromate couple as a nonhazardous brominating agent has been developed.