Dehydroxylated C-3 Alkylation of Indole Accompanied by 1,2-Sulfur Migration

J Org Chem. 2020 May 1;85(9):6206-6215. doi: 10.1021/acs.joc.0c00573. Epub 2020 Apr 21.

Abstract

A metal-free sulfur neighboring group participation C-3 alkylation method between β-sulfur-α-alcohol and indole is documented. Due to its considerable generality and excellent selectivity, this method has been provided a facile access to synthetically useful α-indole-β-functions. Meanwhile, unlike traditional Friedel-Crafts and Mitsunobu reactions, the unique chemoselectivity and regioselectivity may be attributed to a synergetic mechanism with simultaneous C-O cleavage, C-S migration, and C-C formation occurring in the developed reaction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkylation
  • Catalysis
  • Indoles*
  • Molecular Structure
  • Stereoisomerism
  • Sulfur*

Substances

  • Indoles
  • Sulfur