405264-53-1Relevant academic research and scientific papers
Diastereoselective allylation of a chiral imine with allylzinc reagents: Diastereoselective synthesis of a novel broad spectrum carbapenem
Sugimoto,Imamura,Sakoh,Yamada,Morishima
, p. 1747 - 1750 (2007/10/03)
Diastereoselective allylation of chiral imine with allyl-metal reagents was applied to prepare β-amino acid derivative as a key intermediate for the synthesis of a novel carbapenem 1. Combination of the allylzinc reagents and chiral imine, which was derived from L-valine methyl ester as a chiral auxiliary afforded a homoallylamine in good yield with excellent diastereoselectivity.
