Adamantane-1-Carbonyl-Directed C-H Borylation and Hydroxylation of Benzenethiols

Org Lett. 2022 Oct 7;24(39):7163-7167. doi: 10.1021/acs.orglett.2c02858. Epub 2022 Sep 27.

Abstract

A novel route has been described for C-H borylation and hydroxylation of benzenethiols directed by adamantane-1-carbonyl using BBr3. The protocol generates corresponding arylboronic esters and phenols in moderate to excellent yields under metal-free conditions. In addition, the borylated product can be transformed and the directing group can be removed in good yields, which will facilitate the synthesis of structurally diverse benzenethiols.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adamantane*
  • Hydroxylation
  • Phenols
  • Sulfhydryl Compounds

Substances

  • Phenols
  • Sulfhydryl Compounds
  • thiophenol
  • Adamantane