Palladium-catalyzed difluoroalkylative carbonylation of styrenes toward difluoropentanedioates

被引:15
作者
Bao, Zhi-Peng [1 ,2 ]
Zhang, Youcan [1 ]
Wu, Xiao-Feng [1 ,2 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, Dalian Natl Lab Clean Energy, Dalian 116023, Liaoning, Peoples R China
[2] Leibniz Inst Katalyse eV, Albert Einstein Str 29a,1, D-8059 Rostock, Germany
关键词
ALKENES; ACCESS; FLUORINE; ALKYNES; ENONES;
D O I
10.1039/d2sc02665a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The introduction of fluorine atoms into organic molecules is an attractive but challenging topic. In this work, an interesting palladium-catalyzed difluoroalkylative carbonylation of aryl olefins has been developed. A wide range of aryl olefins were transformed into the corresponding difluoropentanedioate compounds with good functional-group tolerance and excellent regioselectivity. Inexpensive ethyl bromodifluoroacetate acts both as a difluoroalkyl precursor and a nucleophile here. Additionally, a scale-up reaction was also performed successfully, and further transformations of the obtained product were shown as well.
引用
收藏
页码:9387 / 9391
页数:5
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