Co(iii)-Catalyzed stereospecific synthesis of (E)-homoallylic alcohols with 4-vinyl-1,3-dioxan-2-ones: late-stage C-H homoallylation of indole derivatives

被引:9
作者
Hu, Hong [1 ]
Xu, Wen-Hua [1 ]
Kang, Wu-Xiang [1 ]
Sun, Wei [1 ]
Sun, Rui [1 ]
Wei, Xiao-Hong [2 ]
Sun, Meng [1 ,3 ]
机构
[1] Northwest Univ, Dept Chem & Mat Sci, Key Lab Synthet & Nat Funct Mol, Minist Educ, Xian 710127, Peoples R China
[2] Northwest Minzu Univ, Coll Chem Engn, Lanzhou 730030, Peoples R China
[3] Dalian Univ Technol, State Key Lab Fine Chem, Dalian 116024, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
STEREOSELECTIVE CARBONYL ALLYLATION; CATALYTIC ASYMMETRIC ALLYLATION; PALLADIUM COMPLEX; DIRECT ADDITION; BOND FORMATION; FUNCTIONALIZATION; ALKENES; 2-VINYLOXIRANE; ACTIVATION; ALDEHYDES;
D O I
10.1039/d1qo00529d
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
An unprecedented Co(iii)-catalyzed stereoselective C-H homoallylation reaction of indole derivatives with 4-vinyl-1,3-dioxan-2-ones to access (E)-homoallylic alcohols has been developed. This protocol features mild reaction conditions, high efficiency, good yields, excellent stereoselectivity, and a broad tolerance towards a variety of functional groups. Notably, the reaction provides a powerful approach for the late-stage C-H homoallylation of indole-based substrates, including bioactive indole derivatives and pharmaceutically relevant indole-containing molecules.
引用
收藏
页码:4459 / 4465
页数:7
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