Cobalt-Catalyzed Enantioselective Dicarbofunctionalization of Acrylates

被引:2
作者
Li, Jiejun [1 ]
Xu, Yi [1 ]
Wan, Xiaolong [1 ]
Shen, Qilong [1 ]
机构
[1] Univ Chinese Acad Sci, Shanghai Inst Organ Chem, Chinese Acad Sci, Key Lab Fluorine & Nitrogen Chem & Adv Mat, Shanghai 200032, Peoples R China
来源
ACS CATALYSIS | 2024年 / 14卷 / 20期
基金
中国国家自然科学基金;
关键词
cobalt; dicarbofunctionalization; asymmetric; alkene; zincate; CROSS-COUPLING REACTIONS; ALPHA-BROMO ESTERS; ARYLATION; PALLADIUM; 1,2-DIFUNCTIONALIZATION; COMPLEXES; DISCOVERY; STYRENES;
D O I
10.1021/acscatal.4c03670
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
Catalytic enantioselective alkene difunctionalization represents a powerful tool for the rapid assembly of complex chiral molecules and has found wide range of applications in synthetic chemistry. Enantioselective control of the newly formed pro-chiral carbon centers using chiral cobalt catalyst, however, remains challenging. Herein, we report the first cobalt-catalyzed enantioselective difunctionalization of industry-relevant acrylates with lithium aryl boronates and alpha,alpha-dialkyl bromoacetate for the preparation of enantioenriched glutaric acid derivatives. Facile transformations of the resulting alpha-aryl esters to other functionalities have been achieved. To further showcase the synthetic utility of the current protocol, application to the enantioselective synthesis of an analog of (-)-preclamol was demonstrated.
引用
收藏
页码:15221 / 15236
页数:16
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