Palladium(0)-Catalyzed Intermolecular Allylic Dearomatization of Indoles by a Formal [4+2] Cycloaddition Reaction

被引:44
作者
Gao, Run-Duo [1 ]
Xu, Qing-Long [1 ]
Zhang, Bo [1 ]
Gu, Yiting [1 ]
Dai, Li-Xin [1 ]
You, Shu-Li [1 ,2 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, 345 Lingling Lu, Shanghai 200032, Peoples R China
[2] Collaborat Innovat Ctr Chem Sci & Engn, Tianjin 300072, Peoples R China
基金
中国国家自然科学基金;
关键词
asymmetric catalysis; dearomatization; indole; indoline; palladium; CATALYZED CASCADE REACTIONS; METHYL VINYL KETONE; 3-SUBSTITUTED INDOLES; ENANTIOSELECTIVE CONSTRUCTION; ASYMMETRIC DEAROMATIZATION; PROPARGYL CARBONATE; N-ALLOC; ACCESS; PYRROLOINDOLINES; ALLYLATION;
D O I
10.1002/chem.201602691
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Bridged indoline derivatives were synthesized by an intermolecular Pd-catalyzed allylic dearomatization reaction of substituted indoles. The reaction between indoles and allyl carbonates bearing a nucleophilic alcohol side-chain proceeds in a cascade fashion, providing bridged indolines in excellent enantioselectivity.
引用
收藏
页码:11601 / 11604
页数:4
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