A new route to functionalised oxazoles

M C Bagley, R T Buck, S L Hind, C J Moody, A M Z Slawin

Research output: Contribution to journalArticlepeer-review

Abstract

Functionalised oxazoles 4 are prepared from amides 1 by rhodium cartenoid N-H insertion reaction to give beta-carbonyl amides 3 followed by cyclodehydration with triphenylphosphine-iodine-triethylamine.

Original languageEnglish
Pages (from-to)825
Number of pages3
JournalSynlett
Issue number9
Publication statusPublished - Sept 1996

Keywords

  • diazocarbonyl
  • rhodium
  • insertion
  • cyclodehydration
  • oxazole
  • H INSERTION REACTIONS
  • DIAZOCARBONYL
  • CARBENOIDS

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