Asymmetric N-heterocyclic carbene catalyzed addition of enals to nitroalkenes: controlling stereochemistry via the homoenolate reactivity pathway to access δ-lactams

J Am Chem Soc. 2013 Jun 12;135(23):8504-7. doi: 10.1021/ja403847e. Epub 2013 May 28.

Abstract

An asymmetric intermolecular reaction between enals and nitroalkenes to yield δ-nitroesters has been developed, catalyzed by a novel chiral N-heterocyclic carbene. Key to this work was the development of a catalyst that favors the δ-nitroester pathway over the established Stetter pathway. The reaction proceeds in high stereoselectivity and affords the previously unreported syn diastereomer. We also report an operationally facile two-step, one-pot procedure for the synthesis of δ-lactams.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkenes / chemistry*
  • Catalysis
  • Heterocyclic Compounds / chemistry*
  • Lactams / chemical synthesis*
  • Lactams / chemistry
  • Methane / analogs & derivatives*
  • Methane / chemistry
  • Molecular Structure
  • Nitro Compounds / chemistry*
  • Stereoisomerism

Substances

  • Alkenes
  • Heterocyclic Compounds
  • Lactams
  • Nitro Compounds
  • carbene
  • Methane