Copper-Catalyzed Oxidative Self-Coupling of -Amino Carbonyl Compounds for the Synthesis of Tetrasubstituted 1,4-Enediones

Copper-Catalyzed Oxidative Self-Coupling of -Amino Carbonyl Compounds for the Synthesis of Tetrasubstituted 1,4-Enediones
复制标题

铜催化氨基羰基化合物氧化自偶联合成四取代 1,4-烯二酮

DOI:
10.1055/s-0037-1611227
复制
发表时间:
2018
期刊:
影响因子:
2
通讯作者:
Xiang Jiannan
Xiang Jiannan
中科院分区:
化学4区
文献类型:
--
作者:
Yia Niannian;Xiong Yi;Huang Qingjun;Yan Ning;Xie Yanjun;Lan Donghui;Yi Ziqi;Au Chak-Tong;Yi Bing;Xiang Jiannan

文献摘要

相似文献

发展了一种铜催化的α-氨基羰基化合物的氧化自偶联反应,通过α-氨基羰基化合物中4个sp3 C-H键的断裂和1个C=C双键的同时形成,以中等至良好的产率合成了四取代的1,4-烯二酮(Z-异构体)。该方法具有原料易得、立体选择性高等优点。
A protocol for the copper-catalyzed oxidative self-coupling of α-amino carbonyl compounds has been developed for the synthesis of tetrasubstituted 1,4-enediones (Z-isomers) in moderate to good yields through the cleavage of four sp3C–H bonds and the simultaneous formation of one C=C double bond in the α-amino carbonyl compound. The strategy has the advantages of using readily available starting materials and of high stereoselectivity.