化学
立体选择性
部分
催化作用
硼酸化
非对映体
钯
邻接
药物化学
芳基
组合化学
立体化学
有机化学
烷基
作者
Yanhui Wang,Qiao Ma,Gavin Chit Tsui
出处
期刊:Organic Letters
[American Chemical Society]
日期:2021-06-11
卷期号:23 (13): 5241-5245
被引量:18
标识
DOI:10.1021/acs.orglett.1c01768
摘要
A highly diastereoselective Pd(0)-catalyzed synthesis of difluorinated 1,3-dienes is described. Symmetrical 1,3-dienes containing a vicinal difluoro moiety can be obtained as single diastereomers from tetrasubstituted gem-difluoroalkenes. The reaction presumably proceeds through a stereoselective twofold Pd-catalyzed Miyaura borylation/Suzuki–Miyaura cross-coupling of the C–F bond. Moreover, modular synthesis of unsymmetrical difluorinated 1,3-dienes is also achievable by the coupling between gem-difluoroalkenes and borylated monofluoroalkenes.
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