双(吲哚基)丙炔(BIPs)的无过渡金属高效合成。

IF 2.8 3区 化学 Q1 CHEMISTRY, ORGANIC Organic & Biomolecular Chemistry Pub Date : 2024-08-28 Epub Date: 2024-08-08 DOI:10.1039/d4ob01017e
Anjali Chaturvedi , Vishal Sharma , Fathimath Nafla CM , Katikam SivaPrasad , Deepak Sharma , Nikhil Kumar , Rushal Chandel , Manpreet Singh , Ravindra K. Rawal , Virender Singh
{"title":"双(吲哚基)丙炔(BIPs)的无过渡金属高效合成。","authors":"Anjali Chaturvedi ,&nbsp;Vishal Sharma ,&nbsp;Fathimath Nafla CM ,&nbsp;Katikam SivaPrasad ,&nbsp;Deepak Sharma ,&nbsp;Nikhil Kumar ,&nbsp;Rushal Chandel ,&nbsp;Manpreet Singh ,&nbsp;Ravindra K. Rawal ,&nbsp;Virender Singh","doi":"10.1039/d4ob01017e","DOIUrl":null,"url":null,"abstract":"<div><p>A transition metal-free approach has been devised for the synthesis of a variety of bis(indolyl)propyne (BIP) derivatives. The strategy involves an iodine-catalyzed cascade condensation of α,β-unsaturated acetylenic aldehydes with diversely substituted indoles. The strategy was applicable to gram scale synthesis and a library of 50 molecules, which were afforded in good to excellent yields (up to 96%), was developed. The salient features of the reaction involve the synthesis of indole based privileged scaffolds in a short reaction time under transition metal-free conditions, with a wide substrate scope and excellent yields under ambient conditions.</p></div>","PeriodicalId":96,"journal":{"name":"Organic & Biomolecular Chemistry","volume":"22 34","pages":"Pages 7039-7051"},"PeriodicalIF":2.8000,"publicationDate":"2024-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Transition metal-free efficient synthesis of bis(indolyl)propynes (BIPs)†\",\"authors\":\"Anjali Chaturvedi ,&nbsp;Vishal Sharma ,&nbsp;Fathimath Nafla CM ,&nbsp;Katikam SivaPrasad ,&nbsp;Deepak Sharma ,&nbsp;Nikhil Kumar ,&nbsp;Rushal Chandel ,&nbsp;Manpreet Singh ,&nbsp;Ravindra K. Rawal ,&nbsp;Virender Singh\",\"doi\":\"10.1039/d4ob01017e\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>A transition metal-free approach has been devised for the synthesis of a variety of bis(indolyl)propyne (BIP) derivatives. The strategy involves an iodine-catalyzed cascade condensation of α,β-unsaturated acetylenic aldehydes with diversely substituted indoles. The strategy was applicable to gram scale synthesis and a library of 50 molecules, which were afforded in good to excellent yields (up to 96%), was developed. The salient features of the reaction involve the synthesis of indole based privileged scaffolds in a short reaction time under transition metal-free conditions, with a wide substrate scope and excellent yields under ambient conditions.</p></div>\",\"PeriodicalId\":96,\"journal\":{\"name\":\"Organic & Biomolecular Chemistry\",\"volume\":\"22 34\",\"pages\":\"Pages 7039-7051\"},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2024-08-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic & Biomolecular Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S147705202400692X\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/8/8 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic & Biomolecular Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S147705202400692X","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/8/8 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0

摘要

我们设计了一种无过渡金属的方法来合成多种双(吲哚基)丙炔(BIP)衍生物。该方法涉及碘催化 α、β-不饱和乙炔醛与多种取代吲哚的级联缩合。该策略适用于克级规模的合成,并开发了一个包含 50 种分子的化合物库,这些化合物的收率从良好到极佳(高达 96%)不等。该反应的显著特点是在无过渡金属条件下,以较短的反应时间合成吲哚类特权支架,底物范围广,环境条件下产率高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

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
Transition metal-free efficient synthesis of bis(indolyl)propynes (BIPs)†

A transition metal-free approach has been devised for the synthesis of a variety of bis(indolyl)propyne (BIP) derivatives. The strategy involves an iodine-catalyzed cascade condensation of α,β-unsaturated acetylenic aldehydes with diversely substituted indoles. The strategy was applicable to gram scale synthesis and a library of 50 molecules, which were afforded in good to excellent yields (up to 96%), was developed. The salient features of the reaction involve the synthesis of indole based privileged scaffolds in a short reaction time under transition metal-free conditions, with a wide substrate scope and excellent yields under ambient conditions.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Organic & Biomolecular Chemistry
Organic & Biomolecular Chemistry 化学-有机化学
CiteScore
5.50
自引率
9.40%
发文量
1056
审稿时长
1.3 months
期刊介绍: Organic & Biomolecular Chemistry is an international journal using integrated research in chemistry-organic chemistry. Founded in 2003 by the Royal Society of Chemistry, the journal is published in Semimonthly issues and has been indexed by SCIE, a leading international database. The journal focuses on the key research and cutting-edge progress in the field of chemistry-organic chemistry, publishes and reports the research results in this field in a timely manner, and is committed to becoming a window and platform for rapid academic exchanges among peers in this field. The journal's impact factor in 2023 is 2.9, and its CiteScore is 5.5.
期刊最新文献
Regio- and enantioselective oxidation by CYP108N12: substrate scope and specificity. Single-step synthesis of 3,5-diazido-1,2,4-triazole: environmentally benign high-performance primary explosives. A straightforward access to specific bisindole systems related to caulersin. Copper-catalyzed selective 1,2-disulfidation of 1,3-dienes. Electrophilic alkene sulfenylation with sulfinate esters.
×
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学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
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