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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Description of the small plastics fragments in marine sediments along the Alang-Sosiya ship-breaking yard, India
TL;DR: In this paper, the accumulation of small plastic debris in the intertidal sediments of the world's largest ship-breaking yard at Alang-Sosiya, India was assessed.
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Copper‐Catalyzed Aerobic Oxidation of Amines to Imines under Neat Conditions with Low Catalyst Loading
TL;DR: In this paper, the copper-catalyzed direct synthesis of imines from amines under mild aerobic conditions is described, which is applicable for the synthesis of various amines from corresponding amines such as benzylic, aliphatic, cyclic secondary, heteroaromatic species and the oxidative condensation of benzylamines with anilines.
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N-chlorosuccinimide-promoted regioselective sulfenylation of imidazoheterocycles at room temperature.
TL;DR: Regioselective sulfenylation of imidazoheterocycles with thiophenols at room temperature is reported and N-chlorosuccinimide is promoted under metal-free conditions with a broad range of substrate scopes.
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l-Proline: An Efficient Catalyst for Transamidation of Carboxamides with Amines
TL;DR: In the presence of a catalytic amount of L-proline (10 mol %), transamidations of carboxamides with amines were achieved under solvent-free conditions and the transamidation process is compatible with a wide range of amines.
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Influence of bases and ligands on the outcome of the Cu(I)-catalyzed oxidative homocoupling of terminal alkynes to 1,4-disubstituted 1,3-diynes using oxygen as an oxidant.
TL;DR: The efficient Cu(I)-catalyzed oxidative homocoupling of terminal alkynes in the presence of a base using an amine as a ligand and oxygen as an oxidant yields the symmetrical 1,3-diynes with yields of up to 99%.