I2-mediated oxidative cyclization for synthesis of substituted indolizines

J Org Chem. 2014 Nov 7;79(21):10641-7. doi: 10.1021/jo5019574. Epub 2014 Oct 10.

Abstract

A direct method for the synthesis of substituted indolizines by means of I2-mediated oxidative tandem cyclization via C-N/C-C bond formation was developed. Various substituted aromatic/aliphatic enolizable aldehydes and 2-pyridylacetates/acetonitrile/acetone proceeded smoothly in this transformation, and the desired products were generated in moderate to good yields.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetonitriles / chemistry*
  • Catalysis
  • Cyclization
  • Indolizines / chemical synthesis*
  • Indolizines / chemistry
  • Iodine / chemistry*
  • Molecular Structure
  • Oxidation-Reduction
  • Pyridines / chemistry*

Substances

  • Acetonitriles
  • Indolizines
  • Pyridines
  • Iodine