Issue 38, 2022

Synthesis of pyrrole disulfides via umpolung of β-ketothioamides

Abstract

A Na2CO3-promoted reaction of β-ketothioamides (KTAs) and cyanoacetates was developed for the synthesis of pyrrole disulfides using air as a green oxidant. This protocol features a broad substrate scope and mild reaction conditions. Preliminary mechanistic studies indicate that the reaction involves a tandem unusual umpolung of KTAs, N-cyclization, tautomerization and oxidative coupling process.

Graphical abstract: Synthesis of pyrrole disulfides via umpolung of β-ketothioamides

Supplementary files

Article information

Article type
Communication
Submitted
21 Aug 2022
Accepted
20 Sep 2022
First published
20 Sep 2022

Org. Biomol. Chem., 2022,20, 7609-7612

Synthesis of pyrrole disulfides via umpolung of β-ketothioamides

X. Meng, W. Guo, G. Nan and M. Li, Org. Biomol. Chem., 2022, 20, 7609 DOI: 10.1039/D2OB01506D

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