钯催化的α、β-不饱和 N-对甲苯磺酰肼与碘醛的级联环化反应:获得 2H-苯并吡喃和 2H-喹啉。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Yiyi Zheng, Xi-Wei Zhu, Yi-Yun Pan, Fei Sun, Long Yao, Xin-Xing Wu
{"title":"钯催化的α、β-不饱和 N-对甲苯磺酰肼与碘醛的级联环化反应:获得 2H-苯并吡喃和 2H-喹啉。","authors":"Yiyi Zheng, Xi-Wei Zhu, Yi-Yun Pan, Fei Sun, Long Yao, Xin-Xing Wu","doi":"10.1039/d4ob01300j","DOIUrl":null,"url":null,"abstract":"<p><p>A palladium-catalyzed cascade reaction of α,β-unsaturated <i>N</i>-tosylhydrazones with iodoarene derivatives containing a nucleophilic group has been developed, which provides facile access to 2<i>H</i>-chromenes and 2<i>H</i>-quinolines, respectively. Additionally, the double Pd-carbene migratory insertion/nucleophilic substitution processes for the synthesis of a ternary heterocyclic skeleton were possible in the developed catalytic system.</p>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-10-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Palladium-catalyzed cascade cyclization of α,β-unsaturated <i>N</i>-tosylhydrazones with iodoarenes: access to 2<i>H</i>-chromenes and 2<i>H</i>-quinolines.\",\"authors\":\"Yiyi Zheng, Xi-Wei Zhu, Yi-Yun Pan, Fei Sun, Long Yao, Xin-Xing Wu\",\"doi\":\"10.1039/d4ob01300j\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>A palladium-catalyzed cascade reaction of α,β-unsaturated <i>N</i>-tosylhydrazones with iodoarene derivatives containing a nucleophilic group has been developed, which provides facile access to 2<i>H</i>-chromenes and 2<i>H</i>-quinolines, respectively. Additionally, the double Pd-carbene migratory insertion/nucleophilic substitution processes for the synthesis of a ternary heterocyclic skeleton were possible in the developed catalytic system.</p>\",\"PeriodicalId\":2,\"journal\":{\"name\":\"ACS Applied Bio Materials\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2024-10-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Bio Materials\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1039/d4ob01300j\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, BIOMATERIALS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d4ob01300j","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 0

摘要

本研究开发了一种钯催化的α,β-不饱和 N-对甲苯磺酰肼与含有亲核基团的碘代芳香烃衍生物的级联反应,可分别简便地获得 2H-苯并吡喃和 2H-喹啉。此外,在所开发的催化系统中,还可以通过双 Pd-碳烯迁移插入/亲核取代过程合成三元杂环骨架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Palladium-catalyzed cascade cyclization of α,β-unsaturated N-tosylhydrazones with iodoarenes: access to 2H-chromenes and 2H-quinolines.

A palladium-catalyzed cascade reaction of α,β-unsaturated N-tosylhydrazones with iodoarene derivatives containing a nucleophilic group has been developed, which provides facile access to 2H-chromenes and 2H-quinolines, respectively. Additionally, the double Pd-carbene migratory insertion/nucleophilic substitution processes for the synthesis of a ternary heterocyclic skeleton were possible in the developed catalytic system.

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
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
×
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