Cu(OTf)2催化含炔酚基双芳基硒化合成含硒螺环和菲

IF 2.5 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Le Guo, Anjia Liu, Hongbo Qi, Lei Gu, Xingyu Yuan, Dongmei Chi and Shufeng Chen
{"title":"Cu(OTf)2催化含炔酚基双芳基硒化合成含硒螺环和菲","authors":"Le Guo, Anjia Liu, Hongbo Qi, Lei Gu, Xingyu Yuan, Dongmei Chi and Shufeng Chen","doi":"10.1039/D5NJ00253B","DOIUrl":null,"url":null,"abstract":"<p >A convenient and practical approach for the synthesis of selenylated spirocyclohexadienones and phenanthrenes through the Cu(OTf)<small><sub>2</sub></small>-promoted, base-controlled selective selenylation of alkynes with diselenides under non-oxidative conditions is described. This reaction demonstrates excellent substrate compatibility and provides a series of aryl-selenide-substituted spirocarbocycles and phenanthrene molecules in moderate to high yields.</p>","PeriodicalId":95,"journal":{"name":"New Journal of Chemistry","volume":" 14","pages":" 5989-5994"},"PeriodicalIF":2.5000,"publicationDate":"2025-03-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Divergent synthesis of selenide-containing spirocarbocycles and phenanthrenes through Cu(OTf)2-promoted selenylation of alkyne-containing phenol-based biaryls†\",\"authors\":\"Le Guo, Anjia Liu, Hongbo Qi, Lei Gu, Xingyu Yuan, Dongmei Chi and Shufeng Chen\",\"doi\":\"10.1039/D5NJ00253B\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >A convenient and practical approach for the synthesis of selenylated spirocyclohexadienones and phenanthrenes through the Cu(OTf)<small><sub>2</sub></small>-promoted, base-controlled selective selenylation of alkynes with diselenides under non-oxidative conditions is described. This reaction demonstrates excellent substrate compatibility and provides a series of aryl-selenide-substituted spirocarbocycles and phenanthrene molecules in moderate to high yields.</p>\",\"PeriodicalId\":95,\"journal\":{\"name\":\"New Journal of Chemistry\",\"volume\":\" 14\",\"pages\":\" 5989-5994\"},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2025-03-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"New Journal of Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2025/nj/d5nj00253b\",\"RegionNum\":3,\"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":"New Journal of Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/nj/d5nj00253b","RegionNum":3,"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

介绍了一种在非氧化条件下由Cu(OTf)2促进、碱控制的炔与二硒化物选择性硒化反应合成硒化螺环己二烯酮和菲的简便易行的方法。该反应证明了良好的底物相容性,并提供了一系列中高产的芳基硒代螺环和菲分子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Divergent synthesis of selenide-containing spirocarbocycles and phenanthrenes through Cu(OTf)2-promoted selenylation of alkyne-containing phenol-based biaryls†

Divergent synthesis of selenide-containing spirocarbocycles and phenanthrenes through Cu(OTf)2-promoted selenylation of alkyne-containing phenol-based biaryls†

A convenient and practical approach for the synthesis of selenylated spirocyclohexadienones and phenanthrenes through the Cu(OTf)2-promoted, base-controlled selective selenylation of alkynes with diselenides under non-oxidative conditions is described. This reaction demonstrates excellent substrate compatibility and provides a series of aryl-selenide-substituted spirocarbocycles and phenanthrene molecules in moderate to high yields.

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
New Journal of Chemistry
New Journal of Chemistry 化学-化学综合
CiteScore
5.30
自引率
6.10%
发文量
1832
审稿时长
2 months
期刊介绍: A journal for new directions in chemistry
×
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