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