Issue 44, 2021

Manganese(iii)-promoted thiocarbonylation of alkylborates with disulfides: synthesis of aliphatic thioesters

Abstract

A Mn(III)-promoted thiocarbonylation procedure toward the synthesis of thioesters has been developed. By employing easily available disulfides and potassium alkyltrifluoroborates as the starting materials, and cheap and non-toxic Mn(OAc)3·2H2O as the promotor, a broad range of thioesters were synthesized in good to excellent yields via radical intermediates.

Graphical abstract: Manganese(iii)-promoted thiocarbonylation of alkylborates with disulfides: synthesis of aliphatic thioesters

Supplementary files

Article information

Article type
Communication
Submitted
06 Oct 2021
Accepted
28 Oct 2021
First published
28 Oct 2021

Org. Biomol. Chem., 2021,19, 9654-9658

Manganese(III)-promoted thiocarbonylation of alkylborates with disulfides: synthesis of aliphatic thioesters

B. Chen and X. Wu, Org. Biomol. Chem., 2021, 19, 9654 DOI: 10.1039/D1OB01960K

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