Nickel-catalyzed thiocarbonylation for the synthesis of thioesters-functionalized 2H-pyrones with sulfonyl chlorides as the sulfur sources

IF 6.5 1区 化学 Q2 CHEMISTRY, PHYSICAL
Chen-Yang Hou , Hucheng Ma , Ruyi Zhao , Xinxin Qi , Xiao-Feng Wu
{"title":"Nickel-catalyzed thiocarbonylation for the synthesis of thioesters-functionalized 2H-pyrones with sulfonyl chlorides as the sulfur sources","authors":"Chen-Yang Hou ,&nbsp;Hucheng Ma ,&nbsp;Ruyi Zhao ,&nbsp;Xinxin Qi ,&nbsp;Xiao-Feng Wu","doi":"10.1016/j.jcat.2024.115764","DOIUrl":null,"url":null,"abstract":"<div><p>An efficient and straightforward protocol for the synthesis of thioesters-functionalized 2<em>H</em>-pyrones has been explored through a nickel-catalyzed thiocarbonylation reaction with sulfonyl chlorides as the sulfur sources. By using Mo(CO)<sub>6</sub> as both CO source and reductant, a diverse set of thioesters-containing 2<em>H</em>-pyrones have been obtained in moderate to good yields. This reaction provides a good supplement for the carbonylative synthesis of thioesters-functionalized 2<em>H</em>-pyrones via a Ni/Mo(CO)<sub>6</sub> catalytic system.</p></div>","PeriodicalId":346,"journal":{"name":"Journal of Catalysis","volume":"439 ","pages":"Article 115764"},"PeriodicalIF":6.5000,"publicationDate":"2024-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Catalysis","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0021951724004779","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

Abstract

An efficient and straightforward protocol for the synthesis of thioesters-functionalized 2H-pyrones has been explored through a nickel-catalyzed thiocarbonylation reaction with sulfonyl chlorides as the sulfur sources. By using Mo(CO)6 as both CO source and reductant, a diverse set of thioesters-containing 2H-pyrones have been obtained in moderate to good yields. This reaction provides a good supplement for the carbonylative synthesis of thioesters-functionalized 2H-pyrones via a Ni/Mo(CO)6 catalytic system.

Abstract Image

镍催化的硫代羰基化反应,以磺酰氯为硫源合成硫代酯官能化的 2H-pyrones
以磺酰氯为硫源,通过镍催化的硫代羰基化反应,探索出了一种高效、简单的合成硫代酯官能化 2H-pyrones 的方法。通过使用 Mo(CO)6 作为 CO 源和还原剂,以中等至良好的产率获得了多种含硫代酯的 2H-pyrones 。该反应为通过 Ni/Mo(CO)6 催化体系羰基合成硫代酯官能化的 2H-pyrones 提供了很好的补充。
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
Journal of Catalysis
Journal of Catalysis 工程技术-工程:化工
CiteScore
12.30
自引率
5.50%
发文量
447
审稿时长
31 days
期刊介绍: The Journal of Catalysis publishes scholarly articles on both heterogeneous and homogeneous catalysis, covering a wide range of chemical transformations. These include various types of catalysis, such as those mediated by photons, plasmons, and electrons. The focus of the studies is to understand the relationship between catalytic function and the underlying chemical properties of surfaces and metal complexes. The articles in the journal offer innovative concepts and explore the synthesis and kinetics of inorganic solids and homogeneous complexes. Furthermore, they discuss spectroscopic techniques for characterizing catalysts, investigate the interaction of probes and reacting species with catalysts, and employ theoretical methods. The research presented in the journal should have direct relevance to the field of catalytic processes, addressing either fundamental aspects or applications of catalysis.
×
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