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Recent Advances in Synthesis of Benzazoles via Imines
Current Organic Chemistry ( IF 2.6 ) Pub Date : 2020-08-31 , DOI: 10.2174/1385272824999200818180845
Ran An 1 , Mengbi Guo 1 , Yingbo Zang 1 , Hang Xu 1 , Zhuang Hou 1 , Chun Guo 1
Affiliation  

Imines, versatile intermediates for organic synthesis, can be exploited for the preparation of diverse classes of biologically active benzazoles. Because of the special characteristics of the C=N bond, imines can be simultaneously used in the synthesis of 1,3-benzazoles and 1,2-benzazoles. With the development of imine synthesis, a variety of novel cascade reactions for benzazole synthesis have been reported in the last decade. Therefore, there is a strong need to elucidate the recent progress in the formation of various classes of benzazoles, including benzimidazoles, benzoxazoles, benzothiazoles, indazoles, and benzisoxazoles, via imines obtained by condensation reactions or oxidative/ redox coupling reactions



中文翻译:

通过亚胺合成苯并恶唑的最新进展

亚胺是有机合成的通用中间体,可用于制备各种类型的具有生物活性的苯并恶唑。由于C = N键的特殊特性,亚胺可同时用于1,3-苯并恶唑和1,2-苯并恶唑的合成。随着亚胺合成的发展,在过去的十年中已经报道了多种用于苯并唑合成的新颖的级联反应。因此,迫切需要阐明通过缩合反应或氧化/氧化还原偶联反应得到的亚胺形成各种类型的苯并恶唑的最新进展,包括苯并咪唑,苯并恶唑,苯并噻唑,吲唑和苯并异恶唑。

更新日期:2020-08-31
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