Synthesis of a bicyclic γ-lactam dipeptide analogue

Jack E. Baldwin, Christopher Hulme, Alison J. Edwards, Christopher J. Schofield, Kevin E.B. Parkes

Research output: Contribution to journalArticle

27 Scopus citations

Abstract

Synthesis of a comformationally restrained bicyclic γ-lactam dipeptide mimetic, involving a diastereoselective bicyclisation reaction is described.

Original languageEnglish (US)
Pages (from-to)1665-1668
Number of pages4
JournalTetrahedron Letters
Volume34
Issue number10
DOIs
StatePublished - Mar 5 1993
Externally publishedYes

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

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  • Cite this

    Baldwin, J. E., Hulme, C., Edwards, A. J., Schofield, C. J., & Parkes, K. E. B. (1993). Synthesis of a bicyclic γ-lactam dipeptide analogue. Tetrahedron Letters, 34(10), 1665-1668. https://doi.org/10.1016/0040-4039(93)85036-V