The palladium-catalyzed arylation of 4H-1,3-dioxin

Takao Sakamoto, Yoshinori Kondo, Hiroshi Yamanaka

Research output: Contribution to journalArticle

50 Citations (Scopus)

Abstract

4H-1,3-Dioxin was firstly arylated by using Heck reaction, and the reaction in the presence of (R)-BINAP gave enantiomerically enriched 4-phenyldioxin which was converted into optically active 1-phenyl-1,3-propanediol.

Original languageEnglish
Pages (from-to)6845-6848
Number of pages4
JournalTetrahedron Letters
Volume33
Issue number45
DOIs
Publication statusPublished - 1992 Nov 3

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

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