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Electrochemical dehydrogenative cyclization of 1,3-dicarbonyl compounds†
Chemical Communications ( IF 4.3 ) Pub Date : 2018-04-19 00:00:00 , DOI: 10.1039/c8cc02472c
Zheng-Jian Wu 1, 2, 3 , Shi-Rui Li 1, 2, 3 , Hao Long 1, 2, 3 , Hai-Chao Xu 1, 2, 3
Affiliation  

The intramolecular C(sp3)–H/C(sp2)–H cross-coupling of 1,3-dicarbonyl compounds has been achieved through Cp2Fe-catalyzed electrochemical oxidation. The key to the success of these dehydrogenative cyclization reactions is the selective activation of the acidic α-C–H bond of the 1,3-dicarbonyl moiety to generate a carbon-centered radical.

中文翻译:

1,3-二羰基化合物的电化学脱氢环化

1,3-二羰基化合物的分子内C(sp 3)–H / C(sp 2)–H交叉偶联是通过Cp 2 Fe催化的电化学氧化实现的。这些脱氢环化反应成功的关键是选择性激活1,3-二羰基部分的酸性α-C–H键以生成一个以碳为中心的自由基。
更新日期:2018-04-19
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