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2022•New Journal of ChemistryRequires access

Hypervalent-iodine-mediated oxidation followed by the acetoxylation/tosylation of α-substituted benzylamines to obtain α-acyloxy/tosyloxy ketones

Bapurao D. Rupanawar, Kishor D. Mane, Gurunath M. Suryavanshi

Open publisher page 3 citations

Abstract

A metal-free and efficient protocol has been developed for sequential oxidation followed by acetoxylation/tosylation of α-alkylbenzylamines for the synthesis of α-acyloxy/tosyloxy ketones using hypervalent iodine( iii ).

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What this paper is about

A metal-free and efficient protocol has been developed for sequential oxidation followed by acetoxylation/tosylation of α-alkylbenzylamines for the synthesis of α-acyloxy/tosyloxy ketones using hypervalent iodine( iii ).

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OpenAlex reports 3 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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Available abstract

A metal-free and efficient protocol has been developed for sequential oxidation followed by acetoxylation/tosylation of α-alkylbenzylamines for the synthesis of α-acyloxy/tosyloxy ketones using hypervalent iodine( iii ).

Key concepts: Chemistry, Hypervalent molecule, Iodine, Organic chemistry, Combinatorial chemistry, Medicinal chemistry

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Hypervalent-iodine-mediated oxidation followed by the acetoxylation/tosylation of α-substituted benzylamines to obtain α-acyloxy/tosyloxy ketones — Research Paper | ScholarLens