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Diastereoselective synthesis of bulky, strongly nucleophilic, and configurationally stable P-stereogenic tricyclic phosphines

Authors :
Gau, David
Rodriguez, Ricardo
Kato, Tsuyoshi
Saffon-Merceron, Nathalie
Baceiredo, Antoine
Source :
Journal of the American Chemical Society. Sept 22, 2010, Vol. 132 Issue 37, 12841-12843
Publication Year :
2010

Abstract

A simple and one-step highly diastereoselective synthesis method was developed to obtain bulky, configurational and air-stable P-chiral tricyclic phosphines 3 exhibiting an exceptionally strong nucleophilic character. The key steps in the method involve the reaction of the stable phosphonium sila-ylide with aryl- and alkyl-substituted acetylene derivatives to obtain enantiomerically pure phosphines.

Details

Language :
English
ISSN :
00027863
Volume :
132
Issue :
37
Database :
Gale General OneFile
Journal :
Journal of the American Chemical Society
Publication Type :
Academic Journal
Accession number :
edsgcl.238593838