Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/4890
Title: Enantioselective synthesis of 1-aryl-2-propenylamines: a new approach to a stereoselective synthesis of the Taxol® side chain.
Authors: Castagnolo, D
Armaroli, S
Corelli, Federico 
Botta, Maurizio 
Issue Date: 2004
Project: None 
Journal: TETRAHEDRON-ASYMMETRY
Abstract: 
A variety of substituted 1-aryl-2-propenylamines of high enantiomeric purity were prepared via lipase-catalysed resolution of the corresponding racemates. (R)-1-Phenyl-2-propenylamine was further synthesised into (2R,3S)-3-benzoylamino-2-hydroxy-3-phenylpropanoic acid methyl ester, the side chain of Taxol®.
Description: 
38699
URI: http://hdl.handle.net/20.500.12779/4890
ISSN: 0957-4166
DOI: 10.1016/j.tetasy.2004.01.035,
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