Enantioselective Construction of Oxindoles Bearing a Quaternary Carbon via Ni-Al Bimetal-Catalyzed Formyl C-H Alkylation

被引:0
|
作者
Wang, Haorui [1 ]
Li, Jiang-Fei [2 ]
Xu, Mengying [1 ]
Zhou, Qi-Lin [1 ]
Xu, Weiwei [1 ]
Ye, Mengchun [1 ]
机构
[1] Nankai Univ, State Key Lab Elementoorgan Chem, Frontiers Sci Ctr New Organ Matter, Coll Chem,Haihe Lab Sustainable Chem Transformat, Tianjin 300071, Peoples R China
[2] Wannan Med Coll, Sch Pharm, Wuhu 241002, Anhui, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
quaternary carbons; C-H alkylation; bimetal; nickel; CHELATION-ASSISTED HYDROESTERIFICATION; SELECTIVE ALKENYLATION; NATURAL-PRODUCTS; BOND FORMATION; LEWIS-ACID; ACTIVATION; RU; ALKENES; METAL; PYRIDINE;
D O I
10.1002/anie.202413652
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Enantioselective transition metal-catalyzed C-H alkylation emerges as one of the most atom- and step-economical routes to chiral quaternary carbons, while big challenges still remain with acyl C-H alkylations. Herein, we use a Ni-Al bimetallic catalyst to facilitate a highly regioselective and highly enantioselective C-H alkylation of formamides with alkenes, constructing various oxindoles bearing a chiral quaternary carbon in up to 94 % yield and up to 95 % ee.
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页数:7
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