Nickel-Catalyzed Multicomponent Assembly of Alkynes toward α-CF3-Alkenes

被引:0
|
作者
Li, Ling [1 ]
Li, Yingmei [1 ]
Yan, Chongchong [1 ]
Zhang, Jian [1 ]
Jiang, Yaojia [1 ]
机构
[1] Guizhou Univ, Ctr R&D Fine Chem, State Key Lab Green Pesticide, Key Lab Green Pesticide & Agr Bioengn,Minist Educ, Guiyang 550025, Peoples R China
基金
中国国家自然科学基金;
关键词
STEREOSELECTIVE-SYNTHESIS; CYCLOADDITION REACTION; N-TOSYLHYDRAZONES; TERMINAL ALKYNES; ACCESS;
D O I
10.1021/acs.orglett.4c01975
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
We disclose an efficient nickel catalytic system for expediting the coupling of alkynes with fluoroalkyl hydrazones and boronic acids, thus facilitating the synthesis of stereospecific alpha-fluoroalkyl-alkene derivatives. 3H-Pyrazoles might be involved as key intermediates through a nitrogen-releasing process, enabling subsequent coupling with boronic acids to afford 1,2-difunctional alkenes in a highly efficient and step-economical fashion. This tandem platform demonstrates broad functional group tolerance, including complex natural products and drug-like molecules.
引用
收藏
页码:5566 / 5570
页数:5
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