Synthesis of 3,4-unsubstituted isoquinolone derivatives from benzimidates and vinylene carbonate via cobalt(iii)-catalyzed C–H activation/cyclization†

IF 2.7 3区 化学 Q1 CHEMISTRY, ORGANIC Organic & Biomolecular Chemistry Pub Date : 2024-11-21 DOI:10.1039/d5ob00319a
Weiyan Xu , Haowen Dang , Huiru Sheng , Jiabin Shen , Min Wang
{"title":"Synthesis of 3,4-unsubstituted isoquinolone derivatives from benzimidates and vinylene carbonate via cobalt(iii)-catalyzed C–H activation/cyclization†","authors":"Weiyan Xu ,&nbsp;Haowen Dang ,&nbsp;Huiru Sheng ,&nbsp;Jiabin Shen ,&nbsp;Min Wang","doi":"10.1039/d5ob00319a","DOIUrl":null,"url":null,"abstract":"<div><div>A cobalt(<span>iii</span>)-catalyzed C–H activation/cyclization of benzimidates and vinylene carbonate has been developed. Various benzimidates showed good compatibility, providing isoquinolone derivatives in moderate to good yields. This strategy employs the inexpensive Co(<span>iii</span>) as the catalyst and provides an efficient and practical solution for the synthesis of medicinally valuable 3,4-unsubstituted isoquinolone derivatives.</div></div>","PeriodicalId":96,"journal":{"name":"Organic & Biomolecular Chemistry","volume":"23 16","pages":"Pages 3836-3840"},"PeriodicalIF":2.7000,"publicationDate":"2024-11-21","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/S1477052025002150","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

Abstract

A cobalt(iii)-catalyzed C–H activation/cyclization of benzimidates and vinylene carbonate has been developed. Various benzimidates showed good compatibility, providing isoquinolone derivatives in moderate to good yields. This strategy employs the inexpensive Co(iii) as the catalyst and provides an efficient and practical solution for the synthesis of medicinally valuable 3,4-unsubstituted isoquinolone derivatives.

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
钴(III)催化C-H活化/环化合成苯并咪甲酸酯和碳酸乙烯基3,4-未取代异喹诺酮衍生物。
研究了钴(III)催化苯并咪甲酸酯和碳酸乙烯酯的碳氢活化/环化反应。各种苯并咪酯具有良好的配伍性,可提供中收率至高收率的异喹诺酮类衍生物。该策略采用廉价的Co(III)作为催化剂,为合成具有药用价值的3,4-未取代异喹诺酮类衍生物提供了一种高效实用的解决方案。
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
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
4-Chloro-2H-chromene-3-carbaldehyde: a valid scaffold in organic synthesis and future molecules for healthcare and energy. Expression of Concern: Total synthesis of the natural product EBC-329. Three-component tandem benzyl-C(sp3)-H functionalization via thermally generated arynes with phenazine. Iron-catalyzed oxidative cleavage of C-N bonds of tertiary amines: syntheses of unsymmetrical ureas from isocyanates. Base-dependent divergent α-cyanation and pyridylation of tertiary amines with cyanoaromatics.
×
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: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