Chiral dienamides-substrates for asymmetric synthesis of amido cyclohexenes

JP Murphy, M Nieuwenhuyzen, K Reynolds, PKS Sarma, PJ Stevenson

Research output: Contribution to journalArticle

31 Citations (Scopus)

Abstract

Chiral dienamides, derived from chiral amines and oxazolidinones, react with electron deficient dienophiles Eo give amino-cyclohexanes with good to excellent de's.

Original languageEnglish
Pages (from-to)9533-9536
Number of pages4
JournalTetrahedron Letters
Volume36
Issue number52
Publication statusPublished - 25 Dec 1995

Keywords

  • DIELS-ALDER REACTIONS
  • ENANTIOSELECTIVE SYNTHESIS
  • 4-NITROCYCLOHEXANONES
  • (+)-LYCORICIDINE
  • SELECTIVITY
  • DERIVATIVES
  • DIENES

Cite this

Murphy, JP., Nieuwenhuyzen, M., Reynolds, K., Sarma, PKS., & Stevenson, PJ. (1995). Chiral dienamides-substrates for asymmetric synthesis of amido cyclohexenes. Tetrahedron Letters, 36(52), 9533-9536.