Cobalt Hydride-Catalyzed Hydroalkynylation of Alkenes with Alkynyl Trifluoroborates

被引:2
|
作者
Guan, Meihui [1 ]
Yin, Ting [1 ]
Wang, Yue [1 ]
Miao, Huanran [1 ]
Zhang, Ge [1 ]
Zhang, Qian [1 ,2 ]
机构
[1] North East Normal Univ, Dept Chem, Jilin Prov Key Lab Organ Funct Mol Design & Synth, Changchun 130024, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China
来源
ACS CATALYSIS | 2024年
基金
中国国家自然科学基金;
关键词
cobalt catalysis; hydrogen atom transfer; hydroalkynylation; alkenes; alkynyl trifluoroborates; radical-polarcrossover; REGIOSELECTIVE HYDROALKYNYLATION; ASYMMETRIC HYDROALKYNYLATION; COMPLEXES; HYDROFUNCTIONALIZATION; HYDROARYLATION; OXIDATIONS; MECHANISM; SECONDARY; ENAMIDES; OLEFINS;
D O I
10.1021/acscatal.4c02211
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A cobalt-catalyzed hydroalkynylation of alkenes with alkynyl trifluoroborates is described, proceeding through a cobalt hydride-mediated radical-polar crossover metal hydrogen-atom-transfer process. This method affords structurally diverse alkynyl-containing compounds in high yields under mild conditions and features a wide substrate scope, good functional group tolerance, and suitability for late-stage functionalization of relatively complex natural products and bioactive molecules. Expanding the scope to alkenyltrifluoroborate salts further increases the utility of the developed methodology. This approach paves an alternative route for radical-involved alkynylation and alkenylation reactions of alkenes with nucleophilic alkynyl/alkenyl reagents.
引用
收藏
页码:9294 / 9301
页数:8
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