Bimodal Glycosyl Donors Protected by 2-O-(ortho-Tosylamido)benzyl Group
2018
Ding, Feiqing | Ishiwata, Akihiro | Ito, Yukishige
A glucosyl donor equipped with C2-o-TsNHbenzyl ether was shown to provide both α- and β-glycosides stereoselectivity, by changing the reaction conditions. Namely, β-glycosides were selectively obtained when the trichloroacetimidate was activated by Tf₂NH. On the other hand, activation by TfOH in Et₂O provided α-glycosides as major products. This “single donor” approach was employed to assemble naturally occurring trisaccharide α-d-Glc-(1→2)-α-d-Glc-(1→6)-d-Glc and its anomers.
显示更多 [+] 显示较少 [-]AGROVOC关键词
书目信息
出版者
American Chemical Society
其它主题
Stereoselectivity; Trisaccharides; Moieties
语言
英语
类型
Journal Article; Text
2024-02-28
MODS