Copper-catalyzed arylation of chlorosilanes with grignard reagents

Eiji Morita, Kei Murakami, Masayuki Iwasaki, Koji Hirano, Hideki Yorimitsu, Koichiro Oshima

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

Nucleophilic substitution reactions of chlorosilanes with aryl Grignard reagents take place efficiently in the presence of copper(I) iodide to afford tetraorganosilanes.

Original languageEnglish
Pages (from-to)1012-1014
Number of pages3
JournalBulletin of the Chemical Society of Japan
Volume82
Issue number8
DOIs
Publication statusPublished - 2009
Externally publishedYes

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Copper
Substitution reactions
cuprous iodide

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

Copper-catalyzed arylation of chlorosilanes with grignard reagents. / Morita, Eiji; Murakami, Kei; Iwasaki, Masayuki; Hirano, Koji; Yorimitsu, Hideki; Oshima, Koichiro.

In: Bulletin of the Chemical Society of Japan, Vol. 82, No. 8, 2009, p. 1012-1014.

Research output: Contribution to journalArticle

Morita, Eiji ; Murakami, Kei ; Iwasaki, Masayuki ; Hirano, Koji ; Yorimitsu, Hideki ; Oshima, Koichiro. / Copper-catalyzed arylation of chlorosilanes with grignard reagents. In: Bulletin of the Chemical Society of Japan. 2009 ; Vol. 82, No. 8. pp. 1012-1014.
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AU - Yorimitsu, Hideki

AU - Oshima, Koichiro

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