通过光氧化催化与二硫代羧酸进行温和绿色的硫代酰化反应

Green Synthesis and Catalysis Pub Date : 2026-02-01 Epub Date: 2024-03-07 DOI:10.1016/j.gresc.2024.02.008
Wen-Chao Gao, Wei Li, Juan Zhang, Hong-Hong Chang, Rong Zhou
{"title":"通过光氧化催化与二硫代羧酸进行温和绿色的硫代酰化反应","authors":"Wen-Chao Gao,&nbsp;Wei Li,&nbsp;Juan Zhang,&nbsp;Hong-Hong Chang,&nbsp;Rong Zhou","doi":"10.1016/j.gresc.2024.02.008","DOIUrl":null,"url":null,"abstract":"<div><div>A photocatalysis process-enabled thioacylation of amines has been developed with eco-friendly feedstock potassium dithiocarboxylates as green thioacyl sources and water as the reaction solvent. The key to the success of this transformation is the light-induced generation of active dithioacyl disulfides as thioacyl donors. This green methodology has been successfully employed for the late-stage thioacylation of various amino compounds including drugs, hormones, amino acids and peptides under mild conditions.</div></div>","PeriodicalId":12794,"journal":{"name":"Green Synthesis and Catalysis","volume":"7 1","pages":"Pages 69-74"},"PeriodicalIF":0.0000,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Mild and green thioacylation with dithiocarboxylates via photoredox catalysis\",\"authors\":\"Wen-Chao Gao,&nbsp;Wei Li,&nbsp;Juan Zhang,&nbsp;Hong-Hong Chang,&nbsp;Rong Zhou\",\"doi\":\"10.1016/j.gresc.2024.02.008\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>A photocatalysis process-enabled thioacylation of amines has been developed with eco-friendly feedstock potassium dithiocarboxylates as green thioacyl sources and water as the reaction solvent. The key to the success of this transformation is the light-induced generation of active dithioacyl disulfides as thioacyl donors. This green methodology has been successfully employed for the late-stage thioacylation of various amino compounds including drugs, hormones, amino acids and peptides under mild conditions.</div></div>\",\"PeriodicalId\":12794,\"journal\":{\"name\":\"Green Synthesis and Catalysis\",\"volume\":\"7 1\",\"pages\":\"Pages 69-74\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2026-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Green Synthesis and Catalysis\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2666554924000280\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/3/7 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Green Synthesis and Catalysis","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666554924000280","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/3/7 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

以环保原料二硫代羧酸钾为绿色硫酰基源,以水为溶剂,研究了光催化氨基硫酰化反应。这种转化成功的关键是光诱导生成活性二硫酰基二硫化物作为硫酰基供体。这种绿色方法已经成功地应用于各种氨基化合物的后期硫酰化,包括药物,激素,氨基酸和肽在温和的条件下。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Mild and green thioacylation with dithiocarboxylates via photoredox catalysis
A photocatalysis process-enabled thioacylation of amines has been developed with eco-friendly feedstock potassium dithiocarboxylates as green thioacyl sources and water as the reaction solvent. The key to the success of this transformation is the light-induced generation of active dithioacyl disulfides as thioacyl donors. This green methodology has been successfully employed for the late-stage thioacylation of various amino compounds including drugs, hormones, amino acids and peptides under mild conditions.
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
CiteScore
14.40
自引率
0.00%
发文量
0
期刊最新文献
N-heterocyclic nitrenium-catalyzed photoreductive radical-polar crossover for alkene dicarbofunctionalization Photochemical nitrene transfer reactions of iminoiodinanes with sulfoxides Stereoselective oxidative C3–N bond dehydrogenation and aromatization of 1-carboxyl substituted tetrahydroisoquinolines employing pipecolate oxidase Modulating regioselectivity of CYP107J3-catalyzed isophorone hydroxylation by disrupting the hydrophobic balance of the substrate binding pocket Visible light induced synthesis of the Benzoyl bioisosteres: bicyclo[1.1.1]pentane-ketone group
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1