Stereoselective Preparation of C-Aryl Glycosides via Visible-Light-Induced Nickel-Catalyzed Reductive Cross-Coupling of Glycosyl Chlorides and Aryl Bromides

被引：35
作者：
Mou, Ze-Dong [1 ,2 ,3 ]
Wang, Jia-Xi [1 ,2 ,3 ]
Zhang, Xia [1 ,2 ,3 ]
Niu, Dawen [1 ,2 ,3 ]
机构：
[1] Sichuan Univ, Dept Emergency, State Key Lab Biotherapy, West China Hosp, Chengdu 610041, Peoples R China
[2] Sichuan Univ, Canc Ctr, West China Hosp, Chengdu 610041, Peoples R China
[3] Sichuan Univ, Sch Chem Engn, Chengdu 610041, Peoples R China
来源：
ADVANCED SYNTHESIS & CATALYSIS | 2021年 / 363卷 / 12期
基金：
中国国家自然科学基金;
关键词：
Carbohydrates; Photoredox catalysis; Nickel; Reductive cross-coupling; Stereoselectivity; Aryl glycosides; PHOTOREDOX CATALYSIS; ARYLATION; INHIBITORS; MECHANISM; SGLT-2; ORGANO; ALKYL;
D O I：
10.1002/adsc.202100343
中图分类号：
O69 [应用化学];
学科分类号：
081704 ;
摘要：
A nickel-catalyzed cross-coupling reaction of glycosyl chlorides with aryl bromides has been developed. The reaction proceeds smoothly under visible-light irradiation and features the use of bench-stable glycosyl chlorides, allowing the highly stereoselective synthesis of C-aryl glycosides.
引用
收藏
页码：3025 / 3029
页数：5
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