An Acid‐Base Promoted Three‐Component Hydrolysis Ring‐Opening Tandem Reaction to Access Thioesters

IF 2.3 4区 化学 Q1 CHEMISTRY, ORGANIC
Asian Journal of Organic Chemistry Pub Date : 2026-08-01 Epub Date: 2026-09-10 DOI:10.1002/ajoc.70519
Sufan Gao, Dan Hu, Xiaonan Guan, Yuanmao Zhang, Lihua Wang, Yulong Li, Chenyi Li
{"title":"An Acid‐Base Promoted Three‐Component Hydrolysis Ring‐Opening Tandem Reaction to Access Thioesters","authors":"Sufan Gao,&nbsp;Dan Hu,&nbsp;Xiaonan Guan,&nbsp;Yuanmao Zhang,&nbsp;Lihua Wang,&nbsp;Yulong Li,&nbsp;Chenyi Li","doi":"10.1002/ajoc.70519","DOIUrl":null,"url":null,"abstract":"<div><div>In this study, a transition metal‐free and thiol‐free method for constructing a series of highly functionalized thioesters has been developed, achieving moderate to good yields from benzothiazolium bromides, aroyl chlorides and H<sub>2</sub>O in a three‐component reaction, via an acid‐base‐promoted hydrolysis ring‐opening tandem reaction process. The present protocol features available starting materials, operational simplicity, and mild reaction conditions.</div></div><div>In this study, a transition metal‐free and thiol‐free method for constructing a series of highly functionalized thioesters has been developed, achieving moderate to good yields from benzothiazolium bromides, aroyl chlorides and H<sub>2</sub>O in a three‐component reaction, via an acid‐base‐promoted hydrolysis ring‐opening tandem reaction process. The present protocol features available starting materials, operational simplicity, and mild reaction conditions.</div><div>A transition metal‐free and thiol‐free method for constructing a series of highly functionalized thioesters has been developed, achieving moderate to good yields from benzothiazolium bromides, aroyl chlorides and H<sub>2</sub>O in a three‐component reaction, via acid‐base‐promoted hydrolysis ring‐opening tandem reaction process.\n<span><figure><span><img><ol><li><span><span>Download: <span>Download high-res image (23KB)</span></span></span></li><li><span><span>Download: <span>Download full-size image</span></span></span></li></ol></span></figure></span></div>","PeriodicalId":130,"journal":{"name":"Asian Journal of Organic Chemistry","volume":"15 8","pages":"Article e70519"},"PeriodicalIF":2.3000,"publicationDate":"2026-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Asian Journal of Organic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S2193580726002278","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/9/10 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0

Abstract

In this study, a transition metal‐free and thiol‐free method for constructing a series of highly functionalized thioesters has been developed, achieving moderate to good yields from benzothiazolium bromides, aroyl chlorides and H2O in a three‐component reaction, via an acid‐base‐promoted hydrolysis ring‐opening tandem reaction process. The present protocol features available starting materials, operational simplicity, and mild reaction conditions.
In this study, a transition metal‐free and thiol‐free method for constructing a series of highly functionalized thioesters has been developed, achieving moderate to good yields from benzothiazolium bromides, aroyl chlorides and H2O in a three‐component reaction, via an acid‐base‐promoted hydrolysis ring‐opening tandem reaction process. The present protocol features available starting materials, operational simplicity, and mild reaction conditions.
A transition metal‐free and thiol‐free method for constructing a series of highly functionalized thioesters has been developed, achieving moderate to good yields from benzothiazolium bromides, aroyl chlorides and H2O in a three‐component reaction, via acid‐base‐promoted hydrolysis ring‐opening tandem reaction process.
  1. Download: Download high-res image (23KB)
  2. Download: Download full-size image
酸-碱促进三组分水解开环串联反应获得硫酯
在本研究中,开发了一种不含过渡金属和不含硫醇的方法来构建一系列高功能化硫酯,通过酸-碱促进的水解开环串联反应过程,以苯并噻唑溴、芳酰氯和水为原料,在三组分反应中获得了中等到较高的产率。本方法的特点是起始原料可用,操作简单,反应条件温和。在本研究中,开发了一种不含过渡金属和不含硫醇的方法来构建一系列高功能化硫酯,通过酸-碱促进的水解开环串联反应过程,以苯并噻唑溴、芳酰氯和水为原料,在三组分反应中获得了中等到较高的产率。本方法的特点是起始原料可用,操作简单,反应条件温和。本文提出了一种不含过渡金属和不含硫醇的方法,通过酸-碱促进水解开环串联反应,以苯并噻唑溴、芳酰氯和水为原料,在三组分反应中获得了中等到较高的产率。下载:下载高清图片(23KB)下载:下载全尺寸图片
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
4.70
自引率
3.70%
发文量
372
期刊介绍: Organic chemistry is the fundamental science that stands at the heart of chemistry, biology, and materials science. Research in these areas is vigorous and truly international, with three major regions making almost equal contributions: America, Europe and Asia. Asia now has its own top international organic chemistry journal—the Asian Journal of Organic Chemistry (AsianJOC) The AsianJOC is designed to be a top-ranked international research journal and publishes primary research as well as critical secondary information from authors across the world. The journal covers organic chemistry in its entirety. Authors and readers come from academia, the chemical industry, and government laboratories.
×
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
小红书