Co/Zn Bimetallic Catalysis Enables Enantioselective Alkynylation of Isatins and α-Ketoesters Using Terminal Alkynes

被引:4
|
作者
Huang, Rui-Zhi [1 ]
Ma, Zhan-Cai [2 ]
Huang, Yuan [2 ]
Zhao, Yu [1 ]
机构
[1] Natl Univ Singapore, Dept Chem, Singapore 117543, Singapore
[2] Xi An Jiao Tong Univ, Sch Pharm, Dept Med Chem, Xian 710061, Peoples R China
来源
JOURNAL OF ORGANIC CHEMISTRY | 2022年 / 88卷 / 12期
基金
中国国家自然科学基金;
关键词
ASYMMETRIC ALKYNYLATION; AROMATIC-ALDEHYDES; ARYLZINC REAGENTS; KETONES; ADDITIONS; SILYLACETYLENES; ALKYLATION; ALCOHOLS; LIGANDS; ACCESS;
D O I
10.1021/acs.joc.2c01369
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
We present herein a novel cobalt/zinc bimetallic catalysis system for the realization of an efficient and enantioselective alkynylation of isatins and alpha-ketoesters using terminal alkynes. By using a simple procedure with all commercially available catalysts, including cobalt bromide, a chiral bisphosphine ligand, and zinc triflate, a range of synthetically useful tertiary propargylic alcohols are accessed with high yields and good enantioselectivities. Control reactions showed that this catalytic system proceeds through activation of the terminal alkyne by zinc triflate and a base, transmetalation from zinc to cobalt, and then the enantio-determining alkynylation of ketones.
引用
收藏
页码:7755 / 7763
页数:9
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