1609945-91-6Relevant articles and documents
Diastereoselective formation of aziridines from diazocarbonyl compounds and N-(O-pivaloylated d-galactosyl)benzylideneamines and ring-opening reactions with p-toluenethiol
Zhao, Yizhou,Wang, Gang,Zhou, Shanshan,Li, Zhongjun,Meng, Xiangbao
, p. 3362 - 3365 (2014)
N-Galactosyl aziridines were synthesized via BF3·OEt 2 promoted addition of carbenes generated from diazocarbonyl compounds with O-pivaloylated β-d-galactosylimines in good yields and high diastereoselectivity. The ring-opening reactions with p-toluenethiol of the aziridines provided enantiometrically pure β-S-substituted phenylalanine derivatives in a highly regioselective manner. the Partner Organisations 2014.