Suzuki-miyaura cross-coupling of benzylic carbonates with arylboronic acids

Ryoichi Kuwano, Masashi Yokogi

Research output: Contribution to journalArticle

109 Citations (Scopus)

Abstract

(Chemical Equation Presented) The cross-coupling of benzylic carbonates with arylboronic acids gave the corresponding diarylmethanes in high yields by use of the palladium catalyst generated in situ from [Pd(n3-C 3H5)Cl]2 and 1,5-bis(diphenylphosphino)pentane (DPPPent). The Suzuki-Miyaura reaction using DPPPent-palladium catalyst is applicable to syntheses of a broad range of functionalized diarylmethanes.

Original languageEnglish
Pages (from-to)945-947
Number of pages3
JournalOrganic Letters
Volume7
Issue number5
DOIs
Publication statusPublished - Mar 3 2005

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Physical and Theoretical Chemistry
  • Organic Chemistry

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