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
StatePublished - Mar 20 2002

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Keywords

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

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

Gradl, S. N., Kennedy-Smith, J. J., Kim, J., & Trauner, D. (2002). A practical variant of the Claisen-Eschenmoser rearrangement: Synthesis of unsaturated morpholine amides. Synlett, (3), 411-414.