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
Stereoselective addition of allylmagnesium chloride to the CN bond of [4.3.0] boron heterobicycles
Furocoumarins of three species of the genus Dorstenia
Stereoselective addition of allylmagnesium chloride to the CN bond of [4.3.0] boron heterobicycles
Structural studies of spiroarsoranes derived from 2-aminophenols
Diastereoselective Synthesis of Spiro-?-lactams via Staudinger Reactio
Facile synthesis of 1,3,6-oxadiazepines from 2,2?-(1,2-ethanediyldiimino)bisphenols