Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/3907
Title: Chiral Allylsilanes Derived From Naturally-occurring Alpha-amino-acids
Authors: M., Franciotti
A., Mordini
Taddei, Maurizio 
Issue Date: 1992
Project: None 
Journal: SYNLETT
Abstract: 
Natural occurring alpha-amino acids, N-butoxycarbonyl protected and converted into the corresponding aldehydes, were transformed into (Z)-alkenes 2-7 by Wittig olefination. Metalation with butyllithium-potassium tert-butoxide gave, after reaction with trimethylsilyl chloride, chiral allylsilanes [e.g., (Z)-(4S)-4-tert-butoxycarbonylamino-6-methyl-1-trimethylsilyl-2-heptene (10)]. The condensation of two of these with acetyl chloride-titanium(IV) chloride is also reported.
Description: 
45941
URI: http://hdl.handle.net/20.500.12779/3907
ISSN: 0936-5214
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