Stereoselective Synthesis of C-Vinyl Glycosides via Nickel-Catalyzed Cross-Electrophile Couplings of 1,2-Glycosyl Orthoesters and Vinyl Halides

被引:3
|
作者
Wang, Xin [1 ,2 ,3 ]
Chen, Anrong [3 ]
Zhao, Shiyin [3 ]
Tao, Qiang [2 ,3 ]
Yang, Bo [3 ]
Zhang, Xing [2 ]
Zhu, Feng [1 ,3 ]
机构
[1] Pingyuan Lab, Xinxiang 453007, Henan, Peoples R China
[2] Nanjing Normal Univ, Sch Food Sci & Pharmaceut Engn, Nanjing 210023, Jiangsu, Peoples R China
[3] Shanghai Jiao Tong Univ, China Frontiers Sci Ctr Transformat Mol FSCTM, Ctr Chem Glycobiol, Shanghai Key Lab Mol Engn Chiral Drugs,Sch Chem &, Shanghai 200240, Peoples R China
基金
上海市自然科学基金; 中国国家自然科学基金; 国家重点研发计划;
关键词
Glycosylation; Nickel catalysis; Cross-electrophile couplings; 1,2-Glycosyl orthoesters; C-C coupling; Stereochemistry; ARYL; OLIGOSACCHARIDE;
D O I
10.1002/cjoc.202400651
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A highly stereoselective nickel-catalyzed cross-electrophile coupling of readily accessible, novel, stable oxygen-based glycosyl radical precursors, specifically 1,2-glycosyl orthoesters, is developed. This approach offers an effective pathway to synthesize diverse C-vinyl glycosides, characterized by good yields, excellent stereoselectivity, mild reaction conditions, a broad substrate scope, and versatile transformations of the resulting products.
引用
收藏
页码:3029 / 3034
页数:6
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