School of Pharmacy , Huazhong University of Science and Technology (HUST) , 13 Hangkong Road , Wuhan , Hubei 430030 , P.R. China.
Research Center for Molecular Recognition and Synthesis, Department of Chemistry , Fudan University , 220 Handan Road , Shanghai 200433 , P.R. China.
Org Lett. 2019 Jun 7;21(11):4008-4013. doi: 10.1021/acs.orglett.9b01200. Epub 2019 May 9.
Azoxyarenes are among important scaffolds in organic molecules. Direct oxidative coupling of primary anilines provides a concise fashion to construct them. However, whether these scaffolds can be prepared from secondary N-alkylanilines is not well explored. Here, we present a catalytic selective oxidative coupling of secondary N-alkylaniline to afford azoxyarene with tungsten catalyst under mild conditions. In addition, azoxy can be viewed as a bioisostere of alkene and amide. Several "azoxyarene analogues" of the corresponding bioactive alkenes and amides showed comparable promising anticancer activities.
偶氮芳烃是有机分子中的重要结构单元之一。直接氧化偶联一级苯胺是构建偶氮芳烃的一种简洁方法。然而,二级 N-烷基亚苯胺能否通过这种方式来制备偶氮芳烃尚未得到充分的研究。在此,我们报道了在温和条件下,使用钨催化剂实现二级 N-烷基亚苯胺的催化选择性氧化偶联,从而制备偶氮芳烃。此外,偶氮芳烃可以看作是烯烃和酰胺的生物等排体。一些相应生物活性烯烃和酰胺的“偶氮芳烃类似物”表现出相当有前途的抗癌活性。