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

IF 2.5 Q2 CHEMISTRY, MULTIDISCIPLINARY
Mohamed Abdel-Megid , Kamelia M. El-mahdy , Azza.M. Elkazak , Sylvia E. Zarif , Mostafa E. Salem
{"title":"Synthetic approaches and biological evaluation of nitrogen bridgehead thiazolo[3,2-a]pyrimidines","authors":"Mohamed Abdel-Megid ,&nbsp;Kamelia M. El-mahdy ,&nbsp;Azza.M. Elkazak ,&nbsp;Sylvia E. Zarif ,&nbsp;Mostafa E. Salem","doi":"10.1016/j.rechem.2024.101807","DOIUrl":null,"url":null,"abstract":"<div><div>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-<em>a</em>]pyrimidines, preparation of the ring system <em>via</em> thioxopyrimidines, thiazoles and other miscellaneous approaches. In addition, some properties related to a broad bioactivity and pharmacology have been reported.</div></div>","PeriodicalId":420,"journal":{"name":"Results in Chemistry","volume":"11 ","pages":"Article 101807"},"PeriodicalIF":2.5000,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Results in Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2211715624005034","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

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.

Abstract Image

氮桥头噻唑并[3,2-a]嘧啶的合成方法和生物学评价
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。
求助全文
约1分钟内获得全文 求助全文
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
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信