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Pd-Catalyzed disilylation: an efficient route to 2,2′-bis(trimethylsilyl)biphenyls via trapping transient dibenzopalladacyclopentadienes with hexamethyldisilane†
Organic Chemistry Frontiers ( IF 5.4 ) Pub Date : 2018-03-13 00:00:00 , DOI: 10.1039/c8qo00189h
Wenguang Li 1, 2, 3, 4, 5 , Genhua Xiao 1, 2, 3, 4, 5 , Guobo Deng 1, 2, 3, 4, 5 , Yun Liang 1, 2, 3, 4, 5
Affiliation  

A palladium-catalyzed disilylation reaction of 2-iodobiphenyls with hexamethyldisilane via trapping transient dibenzopalladacyclopentadienes has been achieved. Diversely functionalized 2,2′-bis(trimethylsilyl)biphenyls have been synthesized in good to excellent yields under mild conditions. Moreover, 2,2′-bis(trimethylsilyl)biphenyls readily transformed into 2,2′-dihalobiphenyls, which could be used to synthesize carbazole, dibenzo[b,d]thiophene and dibenzo[b,d]selenophene polycyclic heteroarenes.

中文翻译:

Pd催化的二烯丙基化:通过用六甲基乙硅烷捕获瞬态二苯并钯四环戊二烯来制备2,2'-双(三甲基甲硅烷基)联苯的有效途径

通过捕获瞬态二苯并钯铝环戊二烯,实现了2-碘联苯与六甲基乙硅烷的钯催化的二烯化反应。已经在温和条件下以良好至优异的产率合成了功能多样的2,2'-双(三甲基甲硅烷基)联苯。此外,2,2'-双(三甲基甲硅烷基)联苯易于转化为2,2'-二卤代联苯,可用于合成咔唑,二苯并[ bd ]噻吩和二苯并[ bd ]硒烯多环杂芳烃。
更新日期:2018-03-13
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