Pd-catalyzed reductive cleavage of alkyl aryl sulfides with triethylsilane that is accelerated by trialkylsilyl chloride

Takehiko Matsumura, Takashi Niwa, Masahisa Nakada

研究成果: Article

27 引用 (Scopus)

抜粋

The palladium-catalyzed reductive cleavage of alkyl aryl sulfides to afford the corresponding arenes in high yield, which is both accelerated and exhibits increased functional group selectivity in the presence of TMSCl, is described. This ligand-free reaction features mild conditions, easy operation, use of readily available reagents, and high functional group selectivity.

元の言語English
ページ(範囲)4313-4316
ページ数4
ジャーナルTetrahedron Letters
53
発行部数33
DOI
出版物ステータスPublished - 2012 8 15

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

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