A detailed investigation of the aza-Prins reaction

Org Biomol Chem. 2010 Mar 7;8(5):1064-80. doi: 10.1039/b915797b. Epub 2010 Jan 5.

Abstract

The development of a Lewis acid-promoted aza-Prins reaction to form piperidines and pyrrolidines is described. Indium trichloride has been found to be a highly successful and mild Lewis acid for promoting this reaction. A thorough mechanistic investigation is described, including the factors that influence the formation of the 5- or 6-membered ring product(s).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cyclization
  • Models, Molecular
  • Molecular Structure
  • Piperidines / chemistry*
  • Pyrrolidines / chemistry*
  • Stereoisomerism

Substances

  • Piperidines
  • Pyrrolidines