Suzuki-Kumada coupling of bromoaroylmethylidenephosphoranes

  • T. Thiemann
  • , K. Umeno
  • , D. Ohira
  • , E. Inohae
  • , T. Sawada
  • , S. Mataka

Research output: Contribution to journalArticlepeer-review

27 Citations (Scopus)

Abstract

Bromoaroylmethylidenephosphoranes 3 are reacted with aryl-and hetarylboronic acids under Suzuki-Kumada conditions to yield biaryl- and arylhetaryl-carbonylmethylidenephosphoranes 4. The reaction can also be run in a one-step procedure from (boromoaroylmethyl)triphenylphosphonium bromides 2. 4 are air-stable phosphoranes that undergo Wittig olefination reactions with aldehydes under benzoic acid catalysis.

Original languageEnglish
Pages (from-to)1067-1070
Number of pages4
JournalNew Journal of Chemistry
Volume23
Issue number11
DOIs
Publication statusPublished - 1999
Externally publishedYes

ASJC Scopus subject areas

  • Catalysis
  • General Chemistry
  • Materials Chemistry

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