Phosphine-catalyzed [4 + 1] annulation between α,β-unsaturated imines and allylic carbonates: synthesis of 2-pyrrolines

J Org Chem. 2011 Apr 1;76(7):2374-8. doi: 10.1021/jo200164v. Epub 2011 Mar 9.

Abstract

In this report, a phosphine-catalyzed [4 + 1] annulation between α,β-unsaturated imines and allylic carbonates is described. This reaction represents the first realization of catalytic [4 + 1] cyclization of 1,3-azadienes with in situ formed phosphorus ylides, which provides highly efficient and diastereoselective synthesis of 2-pyrrolines.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carbonates / chemistry*
  • Catalysis
  • Cyclization
  • Imines / chemistry*
  • Molecular Structure
  • Phosphines / chemistry*
  • Pyrroles / chemical synthesis*
  • Pyrroles / chemistry
  • Stereoisomerism

Substances

  • Carbonates
  • Imines
  • Phosphines
  • Pyrroles
  • pyrroline
  • phosphine