862430-88-4Relevant academic research and scientific papers
Stereoselective synthesis of dienylamines: From amino acids to E-alkene dipeptide isosters
Reginato, Gianna,Gaggini, Francesca,Mordini, Alessandro,Valacchi, Michela
, p. 6791 - 6800 (2005)
A stereoselective approach to dienylamines is described, starting from enantiomerically enriched stannylated allylamines, which are in turn derived from amino acids. Conveniently the procedure allows to introduce diversity at 1-,2- and 4- positions of the final compounds. Conversion to vinylstannane has been extended to dipeptido aldehydes. The possible elaboration of 4-methyl substituted dienylamines to Boc-Gly-Ψ[(E)-CHCH]-(l,d)-Ala and Boc-Phe -Ψ[(E)-CHCH]-(l,d)-Ala dipeptide isosters is also shown.
