Cyclic imine nitro-Mannich/lactamization cascades: a direct stereoselective synthesis of multicyclic piperidinone derivatives

Org Lett. 2008 Oct 2;10(19):4267-70. doi: 10.1021/ol801666w. Epub 2008 Sep 3.

Abstract

An efficient nitro-Mannich/lactamization cascade of gamma-nitro esters with cyclic imines for the preparation of architecturally complex multicyclic piperidinone ring-containing structures has been developed. The reaction is broad in scope and stereoselective and may be coupled to an enantioselective nitroolefin Michael addition reaction as part of a highly enantio- and diastereoselective multicomponent process.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Imines / chemistry*
  • Lactams / chemistry*
  • Piperidines / chemical synthesis*
  • Piperidines / chemistry*
  • Stereoisomerism
  • Substrate Specificity

Substances

  • Imines
  • Lactams
  • Piperidines
  • piperidine