Diastereoselective alkylation of chiral glycinate derivatives containing the ?-phenylethyl group.
Lopez Ruíz, Heraclio
2011
Rodríguez-Garnica Cristina, López-Ruiz Heraclio,* Rojas-Lima Susana, Álvarez - Hernández Alejandro, Tapia-Benavides Rafael, García-López María Concepción. Diastereoselective alkylation of chiral glycinate derivatives containing the ?-phenylethyl group. Journal of the Mexican Chemical Society, 55(3), 148-153. (2011)
Abstract
Novel chiral glycinate derivatives (S)-6 and (S)-7 containing the a-phenylethyl group, were prepared and studied as potentialprecursors of enantiopure a-substituted-a-amino acids. In particular, the alkylation of enolate (S)-7-Li showed substantial (78:22 dr)stereoinduction by the N-(1-phenylethyl)benzamide chiral auxiliary.Addition of DMPU showed no appreciable effect upon the diastereoselectivity
Artículos relacionados
Furocoumarins of three species of the genus Dorstenia
Ylidaddukte der Penteltrichloride
Preparation of N-aryl-substituted spiro-?-lactams via Staudinger cycloaddition
Diastereoselective alkylation of chiral glycinate derivatives containing the ?-phenylethyl group.
Et3, and efficient Mediator for Xanthate Transfer Based Radical Processes.
Structural studies of spiroarsoranes derived from 2-aminophenols
Diastereoselective alkylation of chiral glycinate derivatives containing the ?-phenylethyl group.