照亮芳香族氘化

IF 19.1 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Chem Pub Date : 2024-11-14 DOI:10.1016/j.chempr.2024.09.022
Da Zhao , Tobias Ritter
{"title":"照亮芳香族氘化","authors":"Da Zhao ,&nbsp;Tobias Ritter","doi":"10.1016/j.chempr.2024.09.022","DOIUrl":null,"url":null,"abstract":"<div><div>Late-stage deuteration is a crucial technique in the pharmaceutical industry. Direct aromatic deuteration without the use of directing groups or transition-metal catalysts presents a substantial challenge. Now, through the integration of an interrupted Birch reduction, Liang, Xia, and co-workers have developed a photochemical protocol for the efficient hydrogen isotope exchange to incorporate deuterium into the arenes of pharmaceuticals.</div></div>","PeriodicalId":268,"journal":{"name":"Chem","volume":"10 11","pages":"Pages 3266-3267"},"PeriodicalIF":19.1000,"publicationDate":"2024-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Illuminating aromatic deuteration\",\"authors\":\"Da Zhao ,&nbsp;Tobias Ritter\",\"doi\":\"10.1016/j.chempr.2024.09.022\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Late-stage deuteration is a crucial technique in the pharmaceutical industry. Direct aromatic deuteration without the use of directing groups or transition-metal catalysts presents a substantial challenge. Now, through the integration of an interrupted Birch reduction, Liang, Xia, and co-workers have developed a photochemical protocol for the efficient hydrogen isotope exchange to incorporate deuterium into the arenes of pharmaceuticals.</div></div>\",\"PeriodicalId\":268,\"journal\":{\"name\":\"Chem\",\"volume\":\"10 11\",\"pages\":\"Pages 3266-3267\"},\"PeriodicalIF\":19.1000,\"publicationDate\":\"2024-11-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chem\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2451929424004911\",\"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":"Chem","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2451929424004911","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

后期氘化是制药业的一项关键技术。在不使用定向基团或过渡金属催化剂的情况下直接进行芳香族氘化是一项巨大的挑战。现在,通过整合间断桦木还原法,Liang、Xia 和合作者开发出了一种光化学方案,用于高效的氢同位素交换,将氘掺入药物的芳香族化合物中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Illuminating aromatic deuteration
Late-stage deuteration is a crucial technique in the pharmaceutical industry. Direct aromatic deuteration without the use of directing groups or transition-metal catalysts presents a substantial challenge. Now, through the integration of an interrupted Birch reduction, Liang, Xia, and co-workers have developed a photochemical protocol for the efficient hydrogen isotope exchange to incorporate deuterium into the arenes of pharmaceuticals.
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
Chem
Chem Environmental Science-Environmental Chemistry
CiteScore
32.40
自引率
1.30%
发文量
281
期刊介绍: Chem, affiliated with Cell as its sister journal, serves as a platform for groundbreaking research and illustrates how fundamental inquiries in chemistry and its related fields can contribute to addressing future global challenges. It was established in 2016, and is currently edited by Robert Eagling.
×
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