分子复杂性的快速途径:钯催化的六重多米诺过程获得多环框架**

IF 4.2 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Komal Goel , Gedu Satyanarayana
{"title":"分子复杂性的快速途径:钯催化的六重多米诺过程获得多环框架**","authors":"Komal Goel ,&nbsp;Gedu Satyanarayana","doi":"10.1039/d4cc05380j","DOIUrl":null,"url":null,"abstract":"<div><div>Herein, we present a hitherto unexplored efficient strategy for rapidly constructing structurally constrained and intriguing polycyclic frameworks with two adjacent quaternary centers. Remarkably, this becomes possible through palladium-catalyzed six-fold domino crossover annulations of simple 1,2-bis(2-bromoaryl)ethynes and 1,2-diarylethynes. Notably, this approach demonstrates the synthesis of both C<sub>2</sub>-symmetric and unsymmetric polycyclic products.</div></div>","PeriodicalId":67,"journal":{"name":"Chemical Communications","volume":"61 3","pages":"Pages 536-539"},"PeriodicalIF":4.2000,"publicationDate":"2024-11-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A rapid pathway to molecular complexity: a palladium-catalyzed six-fold domino process to access polycyclic frameworks†\",\"authors\":\"Komal Goel ,&nbsp;Gedu Satyanarayana\",\"doi\":\"10.1039/d4cc05380j\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Herein, we present a hitherto unexplored efficient strategy for rapidly constructing structurally constrained and intriguing polycyclic frameworks with two adjacent quaternary centers. Remarkably, this becomes possible through palladium-catalyzed six-fold domino crossover annulations of simple 1,2-bis(2-bromoaryl)ethynes and 1,2-diarylethynes. Notably, this approach demonstrates the synthesis of both C<sub>2</sub>-symmetric and unsymmetric polycyclic products.</div></div>\",\"PeriodicalId\":67,\"journal\":{\"name\":\"Chemical Communications\",\"volume\":\"61 3\",\"pages\":\"Pages 536-539\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2024-11-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Communications\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S1359734524026107\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Communications","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1359734524026107","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

摘要

在此,我们提出了一种迄今为止尚未探索的有效策略,用于快速构建具有两个相邻四元中心的结构约束和有趣的多环框架。值得注意的是,这可以通过钯催化简单的1,2-双(2-溴芳基)乙炔和1,2-二乙炔的六倍多米诺交叉环实现。值得注意的是,这种方法证明了c2对称和非对称多环产物的合成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A rapid pathway to molecular complexity: a palladium-catalyzed six-fold domino process to access polycyclic frameworks†

A rapid pathway to molecular complexity: a palladium-catalyzed six-fold domino process to access polycyclic frameworks†
Herein, we present a hitherto unexplored efficient strategy for rapidly constructing structurally constrained and intriguing polycyclic frameworks with two adjacent quaternary centers. Remarkably, this becomes possible through palladium-catalyzed six-fold domino crossover annulations of simple 1,2-bis(2-bromoaryl)ethynes and 1,2-diarylethynes. Notably, this approach demonstrates the synthesis of both C2-symmetric and unsymmetric polycyclic products.
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
Chemical Communications
Chemical Communications 化学-化学综合
CiteScore
8.60
自引率
4.10%
发文量
2705
审稿时长
1.4 months
期刊介绍: ChemComm (Chemical Communications) is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world''s major areas of chemical research.
×
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:604180095
Book学术官方微信