Department of Chemistry, Indian Institute of Science Education and Research Bhopal , Bhopal Bypass Road, Bhauri Bhopal, Madhya Pradesh 462066, India.
Org Lett. 2017 Nov 3;19(21):5960-5963. doi: 10.1021/acs.orglett.7b02968.
The coupling of the C(sp)-H bond of ferrocene with toluene avoiding in situ functionalization of both coupling partners has been achieved using palladium and iron dual catalysis. This cross oxidative coupling features regioselectivity to primary and secondary C(sp)-H bonds and chemoselectivity toward the -C(sp)-H over C-I bond of toluene with gram-scale production. It seems Fe(II) catalyst not only stabilizes the generated benzyl radical but also tames its oxidizing behavior, and consequently transfers it to the palladacycle for C-C coupling.
使用钯和铁的双重催化,实现了避免芳环邻位官能团化的二茂铁 C(sp)-H 键与甲苯的偶联。这种交叉氧化偶联具有区域选择性,可作用于伯 C(sp)-H 和仲 C(sp)-H 键,且对甲苯的 -C(sp)-H 键和 C-I 键具有化学选择性,可实现克级规模的生产。Fe(II)催化剂似乎不仅稳定了生成的苄基自由基,还控制了其氧化行为,从而将其转移到钯环中进行 C-C 偶联。