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Synthesis of substituted oxazoles via Pd-catalyzed tandem oxidative cyclization
Organic Chemistry Frontiers ( IF 4.6 ) Pub Date : 2017-09-04 00:00:00 , DOI: 10.1039/c7qo00517b
Wei Zhang 1, 2, 3, 4 , Wenlong Yu 1, 2, 3, 4 , Qiangqiang Yan 1, 2, 3, 4 , Zhanxiang Liu 1, 2, 3, 4 , Yuhong Zhang 1, 2, 3, 4, 5
Affiliation  

A novel method for the synthesis of multisubstituted oxazoles by palladium-catalyzed oxidative cyclization of N-acyl enamides has been developed. The reaction employs readily available iodobenzenes and enamides as the starting materials under mild reaction conditions and provides a reliable way to achieve versatile substituted oxazole derivatives.

中文翻译:

取代的恶唑类的合成通过Pd催化的串联氧化环化

已经开发出一种新的方法,该方法通过钯催化的N-酰基烯酰胺的氧化环化反应来合成多取代的恶唑。该反应在温和的反应条件下采用容易获得的碘代苯和烯酰胺作为起始原料,并提供了一种可靠的方法来获得通用的取代的恶唑衍生物。
更新日期:2017-09-13
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