α-Selective synthesis of 2-deoxy-glycosides and disaccharides

被引:6
|
作者
Yang, Guofang [1 ]
Luo, Xiaosheng [1 ]
Guo, Hong [1 ]
Wang, Qingbing [1 ]
Zhou, Jiafen [1 ]
Huang, Tianyun [1 ]
Tang, Jie [1 ]
Shan, Junjie [2 ]
Zhang, Jianbo [1 ]
机构
[1] East China Normal Univ, Sch Chem & Mol Engn, Shanghai, Peoples R China
[2] Beijing Inst Pharmacol & Toxicol, Dept Pharmacol, Beijing, Peoples R China
基金
上海市自然科学基金;
关键词
2-deoxy glycosides; 2-deoxy disaccharides; TMSOTf; alpha-selective glycosylation; antitumor activity; GLYCOSYLATION; 2-DEOXY; CELLS; 2-DEOXYGLYCOSIDES; OLIGOSACCHARIDES; DIVERSIFICATION; CYTOTOXICITY; DERIVATIVES; GLYCOSIDES; EFFICIENT;
D O I
10.1080/07328303.2018.1439498
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A metal-free catalytic method for the synthesis of 2-deoxy glycosides and disaccharides has been developed using stable 2-deoxy glucosyl and galactosyl acetate donors. They could react with a variety of acceptors in the presence of catalytic amount of TMSOTf at 0 degrees C to form glycosides, glycoconjugates, and disaccharides with excellent alpha-selectivity (> 19:1) and yields (up to 99%) in a short time (0.5 h). With this expedient method, several new compounds against human K562 and SMMC7721 cell lines were obtained and tested with in vitro antitumor bioactivities.
引用
收藏
页码:128 / 152
页数:25
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