The intra- and intermolecular Pauson-Khand reaction promoted by alkyl methyl sulfides

Takumichi Sugihara, Mamiko Yamada, Masahiko Yamaguchi, Mugio Nishizawa

研究成果: Article査読

140 被引用数 (Scopus)

抄録

The Pauson-Khand reaction was promoted by the addition of alkyl methyl sulfides. Among the sulfides, the ones having primary and secondary alkyl groups were more effective than those with tertiary alkyl groups. The intermolecular cyclization with simple alkenes makes the use of n-butyl methyl sulfide as the best method to carry out the stoichiometric Pauson- Khand reaction.

本文言語English
ページ(範囲)771-773
ページ数3
ジャーナルSynlett
6
DOI
出版ステータスPublished - 1999 1月 1

ASJC Scopus subject areas

  • 有機化学

フィンガープリント

「The intra- and intermolecular Pauson-Khand reaction promoted by alkyl methyl sulfides」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。

引用スタイル