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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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Journal Article

A fast and highly efficient method for the synthesis of tertiary amines in aqueous medium

TL;DR: In this paper, a facile and highly efficient method for the synthesis of tertiary amines by the reaction of secondary amines with benzylic bromides and 1,1'-dibromo p/o-xylenes in aqueous dioxane and NaOH is described.
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Recovery of Lac Resin from the Aqueous Effluent of Shellac Industry

TL;DR: In this paper , the authors developed a method for the selective recovery of the lac resin from the alkaline aqueous effluent of shellac manufacturing industry, and the recovered lac resin has been characterized by 13C-NMR, FT-IR and melting point.
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Green Bromine: In situ Generated Catalyst for the Selective Oxidation of Alcohols Using H2O2 as a Benign Oxidant.

TL;DR: Under acid activation, a 5:1 NaBr/NaBrO3 mixture in situ generates Br2/BrOH species which catalyzes the oxidation of benzylic/secondary alcohols by H2O2 to the corresponding aldehydes/ketones.
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Copper‐Catalyzed Denitrogenative Transannulation Reaction of Pyridotriazoles: Synthesis of Imidazo[1,5‐a]pyridines with Amines and Amino Acids.

TL;DR: In this paper, the copper-catalyzed aerobic oxidative synthesis of imidazo[1,5a]pyridines via cascade denitrogenative transannulation reaction of pyridotriazoles with benzylamines with good functional group tolerance is developed.
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Copper-Mediated Synthesis of Pyrazolo[1,5-a]pyridines Through Oxidative Linkage of C—C/N—N Bonds.

TL;DR: In this paper, the pyridyl ester and benzonitriles were furnished under mild conditions from commercially available pyridine carboxylates and pyrinear esters.