Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/4014
Title: 1,3-diastereocontrol With Bromoallenes - Synthesis of Enantiomerically Pure Beta-branched Alpha-amino-acids
Authors: F., Daniello
A., Mann
Taddei, Maurizio 
C. G., Wermuth
Issue Date: 1994
Project: None 
Journal: TETRAHEDRON LETTERS
Abstract: 
Bromoallenes 3a and 3b derived from (D)-Serine undergo S(N)2' alkylation with organo copper reagents to give alkynyl amino alcohol derivatives. These compounds can be further transformed into blanched enantiomerically enriched alpha-amino acids as, for example (L)-Isolcucine and (L)-Alloisoleucine.
Description: 
45954
URI: http://hdl.handle.net/20.500.12779/4014
ISSN: 0040-4039
DOI: 10.1016/S0040-4039(00)77369-2
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