Alternating iodonium-mediated reaction cascades giving indole- and quinoline-containing polycycles

Org Lett. 2008 May 15;10(10):1967-70. doi: 10.1021/ol800202u. Epub 2008 Apr 24.

Abstract

A simple two-step convergent protocol gives direct access to synthetic intermediate A from ortho-iodoanilines. Intermediate A can be treated with NIS in CH2Cl2 to induce novel iodonium mediated domino reaction cascade, which provides direct access to ring-fused indole compounds B. Simply by changing the reaction conditions, this protocol can be directed down an alternative domino reaction cascade to give various ring fused quinoline compounds C.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aniline Compounds / chemistry*
  • Cyclization
  • Indoles / chemistry*
  • Molecular Structure
  • Onium Compounds / chemistry*
  • Polycyclic Compounds / chemical synthesis*
  • Polycyclic Compounds / chemistry
  • Quinolines / chemistry*
  • Stereoisomerism

Substances

  • Aniline Compounds
  • Indoles
  • Onium Compounds
  • Polycyclic Compounds
  • Quinolines