氮桥头噻唑并[3,2-a]嘧啶的合成方法和生物学评价

IF 2.5 Q2 CHEMISTRY, MULTIDISCIPLINARY
Mohamed Abdel-Megid , Kamelia M. El-mahdy , Azza.M. Elkazak , Sylvia E. Zarif , Mostafa E. Salem
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引用次数: 0

摘要

噻唑并嘧啶是由噻唑环和嘧啶环融合在一个分子框架中形成的双环化合物。这两个含有桥头氮原子的杂环系统的融合正吸引着全世界许多药物化学家的关注,以探索该框架的潜力。这篇综述文章试图对含桥头氮的噻唑嘧啶环结构进行文献调查,包括噻唑并[3,2-a]嘧啶、通过噻氧嘧啶、噻唑和其他杂项方法制备环系统。此外,还报告了一些与广泛的生物活性和药理学有关的特性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Synthetic approaches and biological evaluation of nitrogen bridgehead thiazolo[3,2-a]pyrimidines

Synthetic approaches and biological evaluation of nitrogen bridgehead thiazolo[3,2-a]pyrimidines
Thiazolopyrimidines are bicyclic compounds formed by the fusion of thiazole and pyrimidine rings in a single molecular frame. The fusion of these two heterocyclic systems containing bridgehead nitrogen atom is attracting the attention of many medicinal chemists throughout the worldwide to explore the framework for its potential. This review article is an attempt to cover the literature survey of thiazolopyrimidine ring structures with bridging-head nitrogen covers thiazolo[3,2-a]pyrimidines, preparation of the ring system via thioxopyrimidines, thiazoles and other miscellaneous approaches. In addition, some properties related to a broad bioactivity and pharmacology have been reported.
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来源期刊
Results in Chemistry
Results in Chemistry Chemistry-Chemistry (all)
CiteScore
2.70
自引率
8.70%
发文量
380
审稿时长
56 days
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