用Friedel-Crafts反应有机催化不对称合成轴手性和中心手性杂三芳基甲烷。

IF 2.9 3区 化学 Q1 CHEMISTRY, ORGANIC
Yang Min, Hanxiao Shen, Shaoying Huang, Haorui Gu and Xufeng Lin
{"title":"用Friedel-Crafts反应有机催化不对称合成轴手性和中心手性杂三芳基甲烷。","authors":"Yang Min, Hanxiao Shen, Shaoying Huang, Haorui Gu and Xufeng Lin","doi":"10.1039/D5OB00532A","DOIUrl":null,"url":null,"abstract":"<p >A highly enantioselective Friedel–Crafts reaction between C2-unsubstituted naphthyl-indoles and racemic 3-methylated-3<em>H</em>-pyrrolides catalyzed by chiral phosphoric acids has been developed. This reaction provides an efficient and facile route to a series of heterotricyclic triarylmethanes containing axially chiral naphthyl-indole and centrally chiral pyrrole moieties under mild conditions. Moreover, biological evaluation discovered one of these products with promising antitumor activity, and demonstrates its potential application in medicinal chemistry.</p>","PeriodicalId":96,"journal":{"name":"Organic & Biomolecular Chemistry","volume":" 22","pages":" 5359-5372"},"PeriodicalIF":2.9000,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Organocatalytic asymmetric synthesis of axially and centrally chiral heterotriarylmethanes by a Friedel–Crafts reaction†\",\"authors\":\"Yang Min, Hanxiao Shen, Shaoying Huang, Haorui Gu and Xufeng Lin\",\"doi\":\"10.1039/D5OB00532A\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >A highly enantioselective Friedel–Crafts reaction between C2-unsubstituted naphthyl-indoles and racemic 3-methylated-3<em>H</em>-pyrrolides catalyzed by chiral phosphoric acids has been developed. This reaction provides an efficient and facile route to a series of heterotricyclic triarylmethanes containing axially chiral naphthyl-indole and centrally chiral pyrrole moieties under mild conditions. Moreover, biological evaluation discovered one of these products with promising antitumor activity, and demonstrates its potential application in medicinal chemistry.</p>\",\"PeriodicalId\":96,\"journal\":{\"name\":\"Organic & Biomolecular Chemistry\",\"volume\":\" 22\",\"pages\":\" 5359-5372\"},\"PeriodicalIF\":2.9000,\"publicationDate\":\"2025-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic & Biomolecular Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2025/ob/d5ob00532a\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic & Biomolecular Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/ob/d5ob00532a","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0

摘要

研究了手性磷酸催化的2-未取代萘吲哚与3-甲基化3h -外消旋吡咯烷的高度对映选择性Friedel-Crafts反应。该反应为在温和条件下合成一系列含轴手性萘吲哚和中心手性吡咯的杂三环三芳基甲烷提供了一条高效、简便的途径。生物评价发现其中一种具有良好的抗肿瘤活性,并在药物化学方面具有潜在的应用前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Organocatalytic asymmetric synthesis of axially and centrally chiral heterotriarylmethanes by a Friedel–Crafts reaction†

A highly enantioselective Friedel–Crafts reaction between C2-unsubstituted naphthyl-indoles and racemic 3-methylated-3H-pyrrolides catalyzed by chiral phosphoric acids has been developed. This reaction provides an efficient and facile route to a series of heterotricyclic triarylmethanes containing axially chiral naphthyl-indole and centrally chiral pyrrole moieties under mild conditions. Moreover, biological evaluation discovered one of these products with promising antitumor activity, and demonstrates its potential application in medicinal chemistry.

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.
×
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