Photocatalytic decarboxylative selenocyanation of 2-aryloxy and 2-aryl carboxylic acids with N-selenocyanatophthalimide†

Yong Gao , Ruirui Hua , Hongquan Yin , Fu-Xue Chen
{"title":"Photocatalytic decarboxylative selenocyanation of 2-aryloxy and 2-aryl carboxylic acids with N-selenocyanatophthalimide†","authors":"Yong Gao ,&nbsp;Ruirui Hua ,&nbsp;Hongquan Yin ,&nbsp;Fu-Xue Chen","doi":"10.1039/d3qo00347g","DOIUrl":null,"url":null,"abstract":"<div><p>A visible-light-induced decarboxylative selenocyanation reaction of aliphatic carboxylic acids for the formation of C(sp<sup>3</sup>)–SeCN bonds has been developed. The electrophilic <em>N</em>-selenocyanatophthalimide and a pyrylium salt were applied as a SeCN radical precursor and an organic photocatalyst, respectively. The transformation could proceed smoothly without transition metals, oxidants and additional bases, affording the corresponding alkyl selenocyanates in moderate to good yields. This method is characterized by its simplicity, wide substrate scope and mild conditions.</p></div>","PeriodicalId":94379,"journal":{"name":"Organic chemistry frontiers : an international journal of organic chemistry","volume":"10 10","pages":"Pages 2538-2543"},"PeriodicalIF":0.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic chemistry frontiers : an international journal of organic chemistry","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S2052411023007848","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

A visible-light-induced decarboxylative selenocyanation reaction of aliphatic carboxylic acids for the formation of C(sp3)–SeCN bonds has been developed. The electrophilic N-selenocyanatophthalimide and a pyrylium salt were applied as a SeCN radical precursor and an organic photocatalyst, respectively. The transformation could proceed smoothly without transition metals, oxidants and additional bases, affording the corresponding alkyl selenocyanates in moderate to good yields. This method is characterized by its simplicity, wide substrate scope and mild conditions.

Abstract Image

2-芳氧基和2-芳基羧酸与N-硒代氰邻苯二甲酰亚胺的光催化脱羧硒代氰†
开发了一种可见光诱导的脂肪族羧酸脱羧硒代氰反应,用于形成C(sp3)–SeCN键。亲电N-硒代氰基邻苯二甲酰亚胺和丙酮酸盐分别用作SeCN自由基前体和有机光催化剂。在没有过渡金属、氧化剂和额外碱的情况下,转化可以顺利进行,以中等至良好的产率提供相应的烷基硒代氰酸酯。该方法具有简单、底物范围广、条件温和等特点。
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 求助全文
来源期刊
CiteScore
7.80
自引率
0.00%
发文量
0
×
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