2,6-Divinylation of phenols with ethyne

Masahiko Yamaguchi, Mieko Arisawa, Yoshiyuki Kido, Masahiro Hirama

Research output: Contribution to journalArticle

14 Citations (Scopus)

Abstract

Phenols are 2,6-divinylated by treatment with ethyne at 100°C in chlorobenzene in the presence of SnCl4-Bu3N, the divinylation occurring predominantly to exclusively with phenol, alkylphenols and alkoxyphenols; an appropriate amount of the tin reagent and the correct reaction temperature are essential for the divinylation.

Original languageEnglish
Pages (from-to)1663-1664
Number of pages2
JournalChemical Communications
Issue number17
DOIs
Publication statusPublished - 1997 Jan 1

ASJC Scopus subject areas

  • Catalysis
  • Electronic, Optical and Magnetic Materials
  • Ceramics and Composites
  • Chemistry(all)
  • Surfaces, Coatings and Films
  • Metals and Alloys
  • Materials Chemistry

Fingerprint Dive into the research topics of '2,6-Divinylation of phenols with ethyne'. Together they form a unique fingerprint.

Cite this