Application of 2,3-aziridino-γ-lactone methodology toward the enantiospecific synthesis of the (3S,4S)-isomer of dihydroxy-L-glutamic acid
作者:Philippe Dauban、Carole de Saint-Fuscien、Robert H Dodd
DOI:10.1016/s0040-4020(99)00405-6
日期:1999.6
The formal synthesis of benzyl 2,3-aziridino-N-(benzyloxycarbonyl)-2,3-dideoxy-γ-butyrolactone (21) from D-ribose is described. Reaction of 21 with excess benzyl alcohol in the presence of boron trifluoride etherate and hydrogenolysis of the product gave (3S,4S)-dihydroxy-L-glutamic acid ((3S,4S)-3).