An attempt for biaryl coupling reaction of benzyl benzoate derivatives under Ullmann conditions

Hitoshi Abe, Shigemitsu Takeda, Yasuo Takeuchi, Takashi Harayama

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

The biaryl coupling reaction of benzyl benzoate derivatives (3) and (4) was examined with copper(0) reagent. A dimerized product (9) was mainly obtained whereas the desired intramolecularly coupled product (11) was not detected when 3 was employed as the substrate. On the other hand, the reaction of 4 afforded a small amount of the desired lactone (14) although the main product was the dimerized 12.

Original languageEnglish
Pages (from-to)521-528
Number of pages8
JournalHeterocycles
Volume61
DOIs
Publication statusPublished - Dec 31 2003

ASJC Scopus subject areas

  • Analytical Chemistry
  • Pharmacology
  • Organic Chemistry

Fingerprint Dive into the research topics of 'An attempt for biaryl coupling reaction of benzyl benzoate derivatives under Ullmann conditions'. Together they form a unique fingerprint.

  • Cite this