Reactions of Oxazol-5(4H)-ones Involving Organosilicone Reagents (A Review)

IF 0.8 4区 化学 Q4 CHEMISTRY, ORGANIC Russian Journal of Organic Chemistry Pub Date : 2024-07-30 DOI:10.1134/S1070428024050014
V. O. Topuzyan, A. A. Hovannisyan
{"title":"Reactions of Oxazol-5(4H)-ones Involving Organosilicone Reagents (A Review)","authors":"V. O. Topuzyan,&nbsp;A. A. Hovannisyan","doi":"10.1134/S1070428024050014","DOIUrl":null,"url":null,"abstract":"<p>The review summarizes, systematizes, and analyzes the published data concerning the reactions of saturated and unsaturated oxazol-5(4<i>H</i>)-ones with various organosilicon reagents. Examples of the synthesis of heterocyclic compounds, 4,4-disubstituted oxazol-5(4<i>H</i>)-ones, and α,α-disubstituted α-amino acids and their esters by these reactions are considered. For some processes, plausible mechanisms are presented. Examples of the synthesis of biologically active and natural compounds based on reactions involving oxazol-5(4<i>H</i>)-ones and organosilicon reagents are described.</p>","PeriodicalId":766,"journal":{"name":"Russian Journal of Organic Chemistry","volume":null,"pages":null},"PeriodicalIF":0.8000,"publicationDate":"2024-07-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Russian Journal of Organic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1134/S1070428024050014","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0

Abstract

The review summarizes, systematizes, and analyzes the published data concerning the reactions of saturated and unsaturated oxazol-5(4H)-ones with various organosilicon reagents. Examples of the synthesis of heterocyclic compounds, 4,4-disubstituted oxazol-5(4H)-ones, and α,α-disubstituted α-amino acids and their esters by these reactions are considered. For some processes, plausible mechanisms are presented. Examples of the synthesis of biologically active and natural compounds based on reactions involving oxazol-5(4H)-ones and organosilicon reagents are described.

Abstract Image

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
涉及有机硅试剂的恶唑-5(4H)-酮反应(综述)
摘要 本综述总结、系统化并分析了已发表的有关饱和和不饱和噁唑-5(4H)-酮与各种有机硅试剂反应的数据。文中列举了通过这些反应合成杂环化合物、4,4-二取代的噁唑-5(4H)-酮和α,α-二取代的α-氨基酸及其酯的实例。对于某些过程,还提出了似是而非的机理。介绍了基于噁唑-5(4H)-酮和有机硅试剂反应合成具有生物活性的天然化合物的实例。
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
CiteScore
1.40
自引率
25.00%
发文量
139
审稿时长
3-6 weeks
期刊介绍: Russian Journal of Organic Chemistry is an international peer reviewed journal that covers all aspects of modern organic chemistry including organic synthesis, theoretical organic chemistry, structure and mechanism, and the application of organometallic compounds in organic synthesis.
期刊最新文献
Synthesis, Biological Evaluation, and Computational Study of Novel 1,2,3‐Triazole‐Tethered Chalcone Derivatives Iodination of Phenylacetylene and Some Transformations of the Resulting Iodo Derivatives Novel Thiazolinone Derivatives: Synthesis, Biological Evaluation, and In Silico Studies Efficient Route to N-Substituted β-Amido Ketone Scaffold Using Bismuth Nitrate-Catalyzed One-Pot MCR Protocol Efficient Synthesis of 8-Fluoro-10-methyl-3,4-dihydrobenzo[b][1,6]naphthyridine-2(1H)-carboxamides and Their Cytotoxic Activity
×
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