A facile synthesis of 4-arylbutyrolactones via the palladium-catalyzed arylation of 1,3-dioxep-5-ene

Takao Sakamoto, Yoshinori Kondo, Hiroshi Yamanaka

Research output: Contribution to journalArticle

14 Citations (Scopus)

Abstract

1,3-Dioxep-5-ene was arylated by using Heck reaction, and the arylated 1,3-dioxep-4-ene derivatives were easily converted into 4-arylbutyrolactones, intermediates for the synthesis of natural products and biological active compounds.

Original languageEnglish
Pages (from-to)2437-2440
Number of pages4
JournalHeterocycles
Volume36
Issue number11
DOIs
Publication statusPublished - 1993 Nov 1

ASJC Scopus subject areas

  • Analytical Chemistry
  • Pharmacology
  • Organic Chemistry

Fingerprint Dive into the research topics of 'A facile synthesis of 4-arylbutyrolactones via the palladium-catalyzed arylation of 1,3-dioxep-5-ene'. Together they form a unique fingerprint.

  • Cite this