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Synthetic routes for phenazines: an overview

机译:苯吡啶的合成路线:概述

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Phenazines are known to exhibit a diverse range of biological properties, such as antimicrobial, antitumor, antioxidant, antimalarial, neuroprotectant, etc. Owing to their significant applications in both medicinal and industrial fields, the phenazine framework has emerged as a remarkable synthetic target. The most general approaches for synthesis of phenazines include the Wohl-Aue method, Beirut method, condensation of 1,2-diaminobenzenes with 2C-units, reductive cyclization of diphenylamines, oxidative cyclization of 1,2-diaminobenzene/diphenylamines, Pd-catalyzed N-arylation, multicomponent approaches, etc. Advances in the exploitation of synthetic routes for assembly of this scaffold are reported in this review.
机译:已知苯脲素地表现出各种各样的生物学性质,例如抗微生物,抗肿瘤,抗氧化剂,抗疟疾,神经保护剂等由于其药用和工业领域的重要应用,苯吡啶框架被出现为显着的合成靶标。 合成苯酶的最常见方法包括WOHL-AUE方法,贝鲁特方法,1,2-二氨基苯的缩合,具有2C单元,二苯胺的还原环化,1,2-二氨基苯并/二苯胺的氧化环化,PD催化剂 在本次审查中,报道了 - 亚芳,多组分方法等进步。

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