Direct ortho-arylation of N-phenacylpyridinium bromide by palladium-catalyzed C-H-bond activation.

Direct ortho-arylation of N-phenacylpyridinium bromide by palladium-catalyzed C-H-bond activation.
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通过钯催化的 C-H 键活化直接邻位芳基化 N-苯甲酰基溴化吡啶。

DOI:
10.1002/chem.200901399
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发表时间:
2009
期刊:
影响因子:
--
通讯作者:
Yuefei Hu
Yuefei Hu
中科院分区:
--
文献类型:
--
作者:
Jimin Xu;Guolin Cheng;Deyong Su;Yantao Liu;Xinyan Wang;Yuefei Hu

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研究了钯催化溴化N-苯甲酰甲基吡啶的邻位芳基化反应。令人惊讶的N-苯甲酰甲基基团区域选择性地激活吡啶的C-H键并自动从芳基化产物中脱离。动力学同位素效应研究表明,该反应经过C-H键活化途径,由2-苯基吡啶逐步生成2,6-二苯基吡啶。
A novel palladium catalyzed direct ortho-arylation of N-phenacylpyridinium bromide was developed. The amazing N-phenacyl group regioselectively activates the C-H bond of pyridine and automatically departs from the arylated products. A kinetic isotope effect study proved that the reaction went through a C-H-bond activation pathway and 2,6-diphenylpyridine was produced stepwise from 2-phenylpyridine.
DOI: 10.1002/anie.200801465
发表时间: 2008-01-01
影响因子: 16.6
作者:
Billingsley, Kelvin L.;Buchwald, Stephen L.
通讯作者: Buchwald, Stephen L.