Light-induced synthesis of 2H-azirines and its applications in organic chemistry

IF 5.8 2区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Journal of Saudi Chemical Society Pub Date : 2024-03-01 DOI:10.1016/j.jscs.2024.101831
Shibo Lin , Yiwen Chu , Junfeng Deng , Fangqing Xie , Lifeng Zhao
{"title":"Light-induced synthesis of 2H-azirines and its applications in organic chemistry","authors":"Shibo Lin ,&nbsp;Yiwen Chu ,&nbsp;Junfeng Deng ,&nbsp;Fangqing Xie ,&nbsp;Lifeng Zhao","doi":"10.1016/j.jscs.2024.101831","DOIUrl":null,"url":null,"abstract":"<div><p>2<em>H</em>-azirines have represented versatile building motifs in the domain of organic chemistry owing to their excellent reaction activity induced by the high strain of the three-membered ring species. Over the past decades, brilliant achievements have been made in 2<em>H</em>-azirine chemistry involving the construction as well as the transformation of such functional compounds. In the presence of transition metals, strong bases or oxidants, 2<em>H</em>-azirines could be converted into the corresponding products under harsh reaction conditions. Different from traditional catalytic methods, the utilization of photochemistry has proved to be an extremely fascinating protocol that facilitates the construction of 2<em>H</em>-azirine blocks from diverse substrates and further conversion into various derivatives with interesting biological activities. In this regard, more and more light-driven synthetic approaches featuring high efficiency and mild conditions have been developed. Herein, we summarized the accessibility and applications of 2<em>H</em>-azirines as powerful precursors or key intermediates for the synthesis of biologically promising molecules in the presence of photocatalytic conditions.</p></div>","PeriodicalId":16974,"journal":{"name":"Journal of Saudi Chemical Society","volume":"28 2","pages":"Article 101831"},"PeriodicalIF":5.8000,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1319610324000267/pdfft?md5=dee61ceb72f5a13ea66b60b6ba1a4a58&pid=1-s2.0-S1319610324000267-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Saudi Chemical Society","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1319610324000267","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

2H-azirines have represented versatile building motifs in the domain of organic chemistry owing to their excellent reaction activity induced by the high strain of the three-membered ring species. Over the past decades, brilliant achievements have been made in 2H-azirine chemistry involving the construction as well as the transformation of such functional compounds. In the presence of transition metals, strong bases or oxidants, 2H-azirines could be converted into the corresponding products under harsh reaction conditions. Different from traditional catalytic methods, the utilization of photochemistry has proved to be an extremely fascinating protocol that facilitates the construction of 2H-azirine blocks from diverse substrates and further conversion into various derivatives with interesting biological activities. In this regard, more and more light-driven synthetic approaches featuring high efficiency and mild conditions have been developed. Herein, we summarized the accessibility and applications of 2H-azirines as powerful precursors or key intermediates for the synthesis of biologically promising molecules in the presence of photocatalytic conditions.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
光诱导合成 2H-azirines 及其在有机化学中的应用
由于三元环的高应变性所带来的出色反应活性,2H-氮丙啶已成为有机化学领域中用途广泛的构建基团。在过去的几十年中,2H-氮丙啶化学在此类功能化合物的构建和转化方面取得了辉煌的成就。在过渡金属、强碱或氧化剂的作用下,2H-氮丙啶可在苛刻的反应条件下转化为相应的产物。与传统的催化方法不同,光化学的利用已被证明是一种极其迷人的方法,它有助于从不同的底物中构建 2H - 氮丙啶基团,并进一步转化为具有有趣生物活性的各种衍生物。在这方面,越来越多高效、温和的光驱动合成方法被开发出来。在此,我们总结了 2H-氮丙啶作为强大的前体或关键中间体在光催化条件下合成具有生物前景的分子的可及性和应用。
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 去求助
来源期刊
Journal of Saudi Chemical Society
Journal of Saudi Chemical Society CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
8.90
自引率
1.80%
发文量
120
审稿时长
38 days
期刊介绍: Journal of Saudi Chemical Society is an English language, peer-reviewed scholarly publication in the area of chemistry. Journal of Saudi Chemical Society publishes original papers, reviews and short reports on, but not limited to: •Inorganic chemistry •Physical chemistry •Organic chemistry •Analytical chemistry Journal of Saudi Chemical Society is the official publication of the Saudi Chemical Society and is published by King Saud University in collaboration with Elsevier and is edited by an international group of eminent researchers.
期刊最新文献
Ultrasound probe-assisted fabrication of 2,3-disubstituted quinazoline-4(3H)-one framework in the existence of SiO2-decorated nano-scale TiO2 composite and investigating their antibacterial attributes via molecular docking simulations Enhanced antibacterial testing and latent fingerprint detection using dichlorofluorescein-doped carbon dots Development and assessment of vanadium-based metal–organic frameworks for the effective elimination of hazardous pesticides from aqueous solutions: Mechanism of uptake, adsorption capacities, rate of uptake, and enhancement via the Box-Behnken design Novel and reusable magnetic MOF nanocomposite coupled ionic liquid-promoted efficient chemical fixation of CO2 into α-alkylidene cyclic carbonates Continuous processing of JP-10 production: Hydroisomerization of endo-tetrahydrodicyclopentadiene to exo-tetrahydrodicyclopentadiene using a novel bimetal catalyst of Ba/Se supported on TiO2/SO4
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1