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Synthesis of substituted phenols via 1,1-dichloro-2-nitroethene promoted condensation of carbonyl compounds with DMF
Tetrahedron Letters ( IF 1.5 ) Pub Date : 2018-04-30 , DOI: 10.1016/j.tetlet.2018.04.076
Fukai Wang , Wei Wu , Xiaoyong Xu , Xusheng Shao , Zhong Li

A novel and efficient metal-free synthesis of phenolic compounds was developed via coupling cyclization of DMF as a carbon source with active methylene compounds such as 1,3-dicarbonyl compounds with the assistance of 1,1-dichloro-2-nitroethene. The method we used was different from other traditional phenol functionalization methods. In the reaction, the 1,1-dichloro-2-nitroethene as a promoter which unlike our previous research on 1,1-dichloro-2-nitroethene. The method allows the convenient construction of phenolic compounds under mild reaction conditions and moderate yields.



中文翻译:

通过1,1-二氯-2-硝基乙烯合成取代酚促进了羰基化合物与DMF的缩合

通过将作为碳源的DMF与活性亚甲基化合物(例如1,3-二羰基化合物)在1,1-二氯-2-硝基乙烯的辅助下偶联环化,开发了一种新颖,有效的无金属酚类化合物合成方法。我们使用的方法不同于其他传统的苯酚官能化方法。在反应中,1,1-二氯-2-硝基乙烯作为促进剂,这与我们先前对1,1-二氯-2-硝基乙烯的研究不同。该方法允许在温和的反应条件下以中等收率方便地构建酚类化合物。

更新日期:2018-04-30
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