A practical variant of the Claisen-Eschenmoser rearrangement: Synthesis of unsaturated morpholine amides

Stefan N. Gradl, Joshua J. Kennedy-Smith, James Kim, Dirk Trauner

Research output: Contribution to journalArticle

Abstract

A Claisen-Eschenmoser type rearrangement giving rise to unsaturated morpholine-, piperidine- and pyrrolidine amides is described.

Original languageEnglish (US)
Pages (from-to)411-414
Number of pages4
JournalSynlett
Issue number3
DOIs
StatePublished - 2002

Keywords

  • Claisen-Eschenmoser rearrangement
  • Guanacastepene
  • Ketene N,N-acetal
  • Morpholine amides
  • Ring closing metathesis

ASJC Scopus subject areas

  • Organic Chemistry

Fingerprint Dive into the research topics of 'A practical variant of the Claisen-Eschenmoser rearrangement: Synthesis of unsaturated morpholine amides'. Together they form a unique fingerprint.

  • Cite this