Dithiocarbamate mediated thioamidation <i>via</i> C–C single bond cleavage of styrene: study of the protocol in decarbonylative and decarboxylative thioamidations-Reference-Cited by-同舟云学术

Dithiocarbamate mediated thioamidation via C–C single bond cleavage of styrene: study of the protocol in decarbonylative and decarboxylative thioamidations

Published:2024 Issue: Volume: Page:
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Patra Debabrata¹,Saha Amit¹^ORCID

Affiliation:

1. Department of Chemistry, Jadavpur University, Kolkata 700032, India

Abstract

Styrene undergoes transition-metal-free dealkenylative thioamidations by dithiocarbamate anions under aerial conditions. Decarbonylative and decarboxylative thioamidations have also been tested on benzaldehyde, toluene and benzoic acid.

Funder

CouncilofScientific and Industrial Research, India

Science and Engineering Research Board

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2024/QO/D3QO01921G

Reference53 articles.

1. Biosynthesis and Chemical Applications of Thioamides

2. Thioamide Substitution Selectively Modulates Proteolysis and Receptor Activity of Therapeutic Peptide Hormones

3. Rational design of thioamide peptides as selective inhibitors of cysteine protease cathepsin L

4. Semi-synthesis of thioamide containing proteins

5. Direct Radical Copolymerizations of Thioamides To Generate Vinyl Polymers with Degradable Thioether Bonds in the Backbones

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