Directing effect of functional groups in ruthenium-catalyzed addition of substituted acetophonones to an olefin

Motohiro Sonoda, Fumitoshi Kakiuchi, Naoto Chatani, Shinji Murai

Research output: Contribution to journalArticle

58 Citations (Scopus)

Abstract

Ruthenium-catalyzed addition of 3′-methyl-, 3′-trifluoromethyl-, and 3′-N,N-dimethylaminoacetophenones to an olefin proceeds site selectively at 6′ CH bonds to give the 1:1 CH/olefin addition products in high yields. In contrast, the addition of 3′-methoxyacetophenone takes place preferentially at the CH bond at the more congested 2′ position.

Original languageEnglish
Pages (from-to)151-152
Number of pages2
JournalJournal of Organometallic Chemistry
Volume504
Issue number1-2
Publication statusPublished - 1995 Nov 29
Externally publishedYes

Fingerprint

Ruthenium
Alkenes
Functional groups
ruthenium
alkenes
Olefins
methylidyne
products

Keywords

  • Acetophenone
  • Carbon-hydrogen bond cleavage
  • Catalysis
  • Catalytic CH/olefin coupling
  • Ketone
  • Ruthenium

ASJC Scopus subject areas

  • Materials Chemistry
  • Physical and Theoretical Chemistry
  • Organic Chemistry
  • Inorganic Chemistry
  • Biochemistry

Cite this

Directing effect of functional groups in ruthenium-catalyzed addition of substituted acetophonones to an olefin. / Sonoda, Motohiro; Kakiuchi, Fumitoshi; Chatani, Naoto; Murai, Shinji.

In: Journal of Organometallic Chemistry, Vol. 504, No. 1-2, 29.11.1995, p. 151-152.

Research output: Contribution to journalArticle

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