Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/4173
Title: Stereocontrolled synthesis of gamma-branched amino acids. TiCl4 mediated addition of (E)-crotylsilane to N,O-protected serine aldehyde
Authors: F., Daniello
M., Falorni
A., Mann
Taddei, Maurizio 
Issue Date: 1996
Project: None 
Journal: TETRAHEDRON-ASYMMETRY
Abstract: 
The N-Boc derivatives of (2S,3S,4R,6E)-2-amino-3-hydroxy-4-methyl-6-octenoic acid and (2S,4R)-2-amino-4-methyl-hexanoic acid have been prepared using the acetonide of D-Serine aldehyde 1 as a formyl glycine equivalent. The stereochemistry of the y-branch was introduced by reaction of (E)-crotyltrimethylsilane with 1 in the presence of TiCl4 followed by elaboration of the terminal double bond and further transformation of the Serine hydroxymethyl group into a carboxylic acid. Copyright (C) 1996 Elsevier Science Ltd
Description: 
45958
URI: http://hdl.handle.net/20.500.12779/4173
ISSN: 0957-4166
DOI: 10.1016/0957-4166(96)00128-0
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