通过 Cu/SPDO 复合物催化的不对称形式 [3 + 2] 环化从头合成异构苯并呋喃

IF 10.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Fan-Xiao Meng, Xing-Yu Wang, Ka Lu, Ju-Song Yang, Fu-Min Zhang, Ai-Jun Ma, Bao Du, Yong-Qiang Tu
{"title":"通过 Cu/SPDO 复合物催化的不对称形式 [3 + 2] 环化从头合成异构苯并呋喃","authors":"Fan-Xiao Meng,&nbsp;Xing-Yu Wang,&nbsp;Ka Lu,&nbsp;Ju-Song Yang,&nbsp;Fu-Min Zhang,&nbsp;Ai-Jun Ma,&nbsp;Bao Du,&nbsp;Yong-Qiang Tu","doi":"10.1007/s11426-024-2174-x","DOIUrl":null,"url":null,"abstract":"<div><p>Herein, the <i>de novo</i> synthesis of atropisomeric benzofurans through the Cu/spirocyclic-pyrrolidine-oxazoline (SPDO) complex catalyze asymmetric formal [3 + 2] cycloaddition between quinones and ynamides is explored, producing a range of structurally diverse axially chiral benzofurans in satisfactory yields with good to excellent enantioselectivities. Furthermore, density functional theory calculations were applied to explain the possible reaction mechanism.\n</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":772,"journal":{"name":"Science China Chemistry","volume":"68 1","pages":"174 - 180"},"PeriodicalIF":10.4000,"publicationDate":"2024-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"De novo synthesis of atropisomeric benzofurans via Cu/SPDO complex catalyzed asymmetric formal [3 + 2] annulation\",\"authors\":\"Fan-Xiao Meng,&nbsp;Xing-Yu Wang,&nbsp;Ka Lu,&nbsp;Ju-Song Yang,&nbsp;Fu-Min Zhang,&nbsp;Ai-Jun Ma,&nbsp;Bao Du,&nbsp;Yong-Qiang Tu\",\"doi\":\"10.1007/s11426-024-2174-x\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Herein, the <i>de novo</i> synthesis of atropisomeric benzofurans through the Cu/spirocyclic-pyrrolidine-oxazoline (SPDO) complex catalyze asymmetric formal [3 + 2] cycloaddition between quinones and ynamides is explored, producing a range of structurally diverse axially chiral benzofurans in satisfactory yields with good to excellent enantioselectivities. Furthermore, density functional theory calculations were applied to explain the possible reaction mechanism.\\n</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>\",\"PeriodicalId\":772,\"journal\":{\"name\":\"Science China Chemistry\",\"volume\":\"68 1\",\"pages\":\"174 - 180\"},\"PeriodicalIF\":10.4000,\"publicationDate\":\"2024-09-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Science China Chemistry\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s11426-024-2174-x\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Science China Chemistry","FirstCategoryId":"1","ListUrlMain":"https://link.springer.com/article/10.1007/s11426-024-2174-x","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

摘要

本文探讨了通过 Cu/螺环吡咯烷-噁唑啉(SPDO)复合物催化醌类化合物和炔酰胺之间的不对称形式 [3 + 2] 环加成从头合成异构体苯并呋喃的方法,以令人满意的产率和良好至卓越的对映选择性制备出一系列结构多样的轴向手性苯并呋喃。此外,还应用密度泛函理论计算解释了可能的反应机理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
De novo synthesis of atropisomeric benzofurans via Cu/SPDO complex catalyzed asymmetric formal [3 + 2] annulation

Herein, the de novo synthesis of atropisomeric benzofurans through the Cu/spirocyclic-pyrrolidine-oxazoline (SPDO) complex catalyze asymmetric formal [3 + 2] cycloaddition between quinones and ynamides is explored, producing a range of structurally diverse axially chiral benzofurans in satisfactory yields with good to excellent enantioselectivities. Furthermore, density functional theory calculations were applied to explain the possible reaction mechanism.

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
Science China Chemistry
Science China Chemistry CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
14.40
自引率
7.30%
发文量
3787
审稿时长
2.2 months
期刊介绍: Science China Chemistry, co-sponsored by the Chinese Academy of Sciences and the National Natural Science Foundation of China and published by Science China Press, publishes high-quality original research in both basic and applied chemistry. Indexed by Science Citation Index, it is a premier academic journal in the field. Categories of articles include: Highlights. Brief summaries and scholarly comments on recent research achievements in any field of chemistry. Perspectives. Concise reports on thelatest chemistry trends of interest to scientists worldwide, including discussions of research breakthroughs and interpretations of important science and funding policies. Reviews. In-depth summaries of representative results and achievements of the past 5–10 years in selected topics based on or closely related to the research expertise of the authors, providing a thorough assessment of the significance, current status, and future research directions of the field.
×
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