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Synthesis of 1,4‐Benzothiazines via KI/DMSO/O2‐Mediated Three‐Component Oxidative Cyclization/Coupling
Advanced Synthesis & Catalysis ( IF 5.4 ) Pub Date : 2020-03-25 , DOI: 10.1002/adsc.202000201
Jinwu Zhao 1 , Zhigao Luo 1 , Jingxiu Xu 1
Affiliation  

A three‐component transition‐metal‐free aerobic method for the generation of 1,4‐benzothiazines is reported herein. The KI/DMSO/O2 system was found to be effective for the oxidative cyclization/coupling of 2‐aminobenzenethiols, anilines, and methylketones. Hence, various structurally important imino 1,4‐benzothiazines were assembled with broad functional group tolerance. Mechanistic studies revealed an initial oxidation of ketone α C−H bonds by the KI/DMSO/O2 oxidative system.

中文翻译:

通过KI / DMSO / O2介导的三组分氧化环化/偶联合成1,4-苯并噻嗪

本文报道了一种用于生成1,4-苯并噻嗪的三组分无过渡金属好氧方法。发现KI / DMSO / O 2系统对于2-氨基苯硫醇,苯胺和甲基酮的氧化环化/偶联有效。因此,组装了具有重要官能团耐受性的各种结构上重要的亚氨基1,4-苯并噻嗪。机理研究表明,KI / DMSO / O 2氧化体系使酮αC-H键初步氧化。
更新日期:2020-03-25
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