Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/4375
Title: Stereoselective addition of phenyl selenyl chloride to methoxy alkenes derived from N-protected chiral alpha-amino acids.
Authors: M., Demarcus
S. N., Filigheddu
A., Mann
Taddei, Maurizio 
Issue Date: 1999
Project: None 
Journal: TETRAHEDRON LETTERS
Abstract: 
(E)-Methoxy alkenes derived from N-Boc or NCbz alpha-amino acids undergo stereoselective addition of phenyl selenyl chloride in the presence of Ti(Oi-Pr)(4) and LiCl to give the corresponding phenylselenyl aldehydes that can be easily transformed into new enantiomericalIy pure amino acids containing an aziridine ring. (C) 1999 Elsevier Science Ltd. All rights reserved.
Description: 
45977
URI: http://hdl.handle.net/20.500.12779/4375
ISSN: 0040-4039
DOI: 10.1016/S0040-4039(99)00761-3
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