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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.
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页码:5566 / 5570
页数:5
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