Nitro-Mannich/lactamization cascades for the direct stereoselective synthesis of pyrrolidin-2-ones

Org Lett. 2009 Oct 15;11(20):4512-5. doi: 10.1021/ol901640v.

Abstract

An efficient three-component nitro-Mannich/lactamization cascade of methyl 3-nitropropanoate with in situ formed acyclic imines for the direct preparation of pyrrolidinone derivatives has been developed. The reaction is easy to perform, broad in scope, and highly diastereoselective and may be extended to cyclic imines allowing the direct formation of polycyclic pyrrolidinone derivatives.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aldehydes / chemistry
  • Lactams / chemistry*
  • Mannich Bases / chemistry*
  • Nitro Compounds / chemistry*
  • Pyrrolidinones / chemical synthesis*
  • Pyrrolidinones / chemistry*
  • Stereoisomerism
  • Substrate Specificity

Substances

  • Aldehydes
  • Lactams
  • Mannich Bases
  • Nitro Compounds
  • Pyrrolidinones