Volume 4, Issue 5 pp. 475-486
Dedicated Article
Full Access

Synthesis and reactions of optically pure cyclohexyl(o-methoxyphenyl)phosphine-borane and t-butyl-(o-methoxyphenyl)phosphine-borane

Tsuneo Imamoto

Corresponding Author

Tsuneo Imamoto

Department of Chemistry, Faculty of Science, Chiba University, Inage, Chiba 263, Japan

Department of Chemistry, Faculty of Science, Chiba University, Inage, Chiba 263, JapanSearch for more papers by this author
Masatoshi Matsuo

Masatoshi Matsuo

Department of Chemistry, Faculty of Science, Chiba University, Inage, Chiba 263, Japan

Search for more papers by this author
Taro Nonomura

Taro Nonomura

Department of Chemistry, Faculty of Science, Chiba University, Inage, Chiba 263, Japan

Search for more papers by this author
Kuniyuki Kishikawa

Kuniyuki Kishikawa

Department of Chemistry, Faculty of Science, Chiba University, Inage, Chiba 263, Japan

Search for more papers by this author
Masao Yanagawa

Masao Yanagawa

Department of Chemistry, Faculty of Science, Chiba University, Inage, Chiba 263, Japan

Search for more papers by this author
First published: October 1993
Citations: 41

Dedicated to Prof. Antonino Fava on the occasion of his seventieth birthday.

Abstract

Cyclohexyl(o-methoxyphenyl)menthyloxyphosphineborane and t-butyl(o-methoxyphenyl)menthyloxyphosphine-borane were prepared from dichlorocyclohexylphosphine and t-butyldichlorophosphine by successive treatments with (−)-menthol, o-methoxyphenylmagnesium bromide, and borane-THF complex. The separated pure diastereomers of each of the compounds underwent reaction with lithium naphthalenide to afford optically pure cyclohexyl(o-methoxyphenyl)phosphine-borane and t-butyl(o-methoxyphenyl)phosphine-borane, respectively. These secondary phosphine-boranes reacted readily with various electrophiles in the presence of bases with virtually net retention of configuration. A new chiral phosphine ligand, (S,S)-1,2-bis[cyclohexyl(o-methoxyphenyl)phosphino]ethane was synthesized via the optically pure phosphine-boranes.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.