Platinum-catalyzed domino reaction with benziodoxole reagents for accessing benzene-alkynylated indoles

Angew Chem Int Ed Engl. 2015 Apr 27;54(18):5438-42. doi: 10.1002/anie.201412321. Epub 2015 Mar 10.

Abstract

Indoles are omnipresent in natural products, bioactive molecules, and organic materials. Consequently, their synthesis or functionalization are important fields of research in organic chemistry. Most works focus on installation or modification of the pyrrole ring. To access benzene-ring-functionalized indoles with an unsubstituted pyrrole ring remains more challenging. Reported herein is a platinum-catalyzed cyclization/alkynylation domino process to selectively obtain C5- or C6-functionalized indoles starting from easily available pyrroles. The work combines, for the first time, a platinum catalyst with ethynylbenziodoxole hypervalent iodine reagents in a domino process for the synthesis of polyfunctionalized arene rings and gives access to important building blocks for the synthesis of bioactive compounds and organic materials.

Keywords: alkynes; cyclization; heterocycles; hypervalent compounds; platinum.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkynes / chemistry*
  • Catalysis
  • Cyclization
  • Hydrogen Bonding
  • Indoles / chemical synthesis*
  • Indoles / chemistry
  • Iodobenzenes
  • Iodobenzoates / chemistry*
  • Molecular Structure
  • Platinum / chemistry*

Substances

  • Alkynes
  • Indoles
  • Iodobenzenes
  • Iodobenzoates
  • o-iodoxybenzoic acid
  • Platinum