Synthesis of pyrrole disulfides via umpolung of β-ketothioamides

Org Biomol Chem. 2022 Oct 5;20(38):7609-7612. doi: 10.1039/d2ob01506d.

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cyclization
  • Disulfides*
  • Molecular Structure
  • Oxidants
  • Pyrroles*

Substances

  • Disulfides
  • Oxidants
  • Pyrroles