Palladium/-catalyzed enantioselective cascade Heck/intermolecular C(sp2)-H alkylation reaction

被引:6
|
作者
Fang, Chao [1 ]
Wang, Quan-Pu [1 ]
Xu, Bing [1 ,3 ]
Zhang, Zhan-Ming [1 ,2 ]
Zhang, Junliang [1 ,3 ,4 ]
机构
[1] Fudan Univ, Dept Chem, Shanghai 200438, Peoples R China
[2] Fudan Zhangjiang Inst, Shanghai 201203, Peoples R China
[3] Zhuhai Fudan Innovat Inst, Zhuhai 519000, Guangdong, Peoples R China
[4] Henan Normal Univ, Sch Chem & Chem Engn, Xinxiang 453007, Henan, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金; 国家重点研发计划;
关键词
H FUNCTIONALIZATION; BOND;
D O I
10.1039/d4sc00262h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Palladium-catalyzed enantioselective domino Heck/intramolecular C-H functionalization reaction, as a valuable strategy for creating molecular diversity, has remained a prominent challenge. Here, we describe a Pd/XuPhos catalyst for asymmetric domino Heck/intermolecular C-H alkylation of unactivated alkenes with diverse polyfluoro- and heteroarenes in a highly chemo- and enantioselective manner. This process enables efficient synthesis of various dihydrobenzofurans, indolines and indanes, which are of interest in pharmaceutical research and other areas. Late-stage modifications of the core structures of natural products are also well showcased. Moreover, synthetic transformations create a valuable platform for preparing a series of functionalized molecules. Several control experiments for mechanistic study are conducted to pursue a further understanding of the reaction.
引用
收藏
页码:5573 / 5580
页数:8
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