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Efficient functionalization of olefins by arylsilanes catalyzed by palladium anionic complexes
Journal of Molecular Catalysis A: Chemical Pub Date : 2016-07-12 , DOI: 10.1016/j.molcata.2016.07.023
E. Silarska , M. Majchrzak , B. Marciniec , A.M. Trzeciak

The coupling of organosilanes and different olefins was performed efficiently in the presence of anionic complexes, [CA]2[PdX4] and [CA]2[Pd2X6], where CA = imidazolium or pyridinium cation. The reaction proceeds according to a Pd(II)-mediated pathway, and Cu(OAc)2 acts as the re-oxidant of Pd(0) formed during the catalytic process. High product yields were obtained for differently substituted olefins at 80 °C in 4 h. Styrylsilanes reacted in the same conditions giving unsymmetrical 1,3-dienes.



中文翻译:

钯阴离子配合物催化芳基硅烷对烯烃的高效官能化

有机硅烷和不同烯烃的偶联在阴离子络合物[CA] 2 [PdX 4 ]和[CA] 2 [Pd 2 X 6 ]的存在下有效进行,其中CA =咪唑鎓或吡啶鎓阳离子。反应根据Pd(II)介导的途径进行,Cu(OAc)2充当催化过程中形成的Pd(0)的再氧化剂。在80°C下4小时内,不同取代的烯烃获得了较高的产物收率。苯乙烯基硅烷在相同条件下反应,生成不对称的1,3-二烯。

更新日期:2016-07-12
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