Total synthesis of (±)-mersicarpine following a 6- exo-trig radical cyclization

Org Biomol Chem. 2022 Aug 10;20(31):6193-6195. doi: 10.1039/d2ob00620k.

Abstract

Described is a total synthesis of racemic mersicarpine from diethyl 4-oxopimelate. The synthetic route takes advantage of a 2-indolyl radical cyclization to construct the pyrido[1,2-a]indole scaffold bearing the all-carbon quaternary stereocenter.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cyclization
  • Indole Alkaloids*
  • Molecular Structure
  • Stereoisomerism

Substances

  • Indole Alkaloids
  • mersicarpine