稀土催化α-C(sp3)-氢硅烷分子内硅化反应合成[1,3]-硫代硅烷

IF 4.2 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Kun An, Mengqing Liu, Jingxia Wang, Masayoshi Nishiura, Xuefeng Cong, Zhaomin Hou
{"title":"稀土催化α-C(sp3)-氢硅烷分子内硅化反应合成[1,3]-硫代硅烷","authors":"Kun An, Mengqing Liu, Jingxia Wang, Masayoshi Nishiura, Xuefeng Cong, Zhaomin Hou","doi":"10.1039/d5cc04330a","DOIUrl":null,"url":null,"abstract":"The intramolecular α-C(sp3)-H silylation of alkyl sulfides with hydrosilanes has been achieved for the first time by the use of halfsandwich rare-earth catalysts. This transformation smoothly proceeds without the need for a H2 acceptor, offering an efficient and selective protocol for the synthesis of a new family of heterocyclic [1,3]-thiasilolanes.","PeriodicalId":67,"journal":{"name":"Chemical Communications","volume":"115 1","pages":""},"PeriodicalIF":4.2000,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis of [1,3]-thiasilolanes via rare-earth-catalysed intramolecular α-C(sp3)-H silylation of alkyl sulphides with hydrosilanes\",\"authors\":\"Kun An, Mengqing Liu, Jingxia Wang, Masayoshi Nishiura, Xuefeng Cong, Zhaomin Hou\",\"doi\":\"10.1039/d5cc04330a\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The intramolecular α-C(sp3)-H silylation of alkyl sulfides with hydrosilanes has been achieved for the first time by the use of halfsandwich rare-earth catalysts. This transformation smoothly proceeds without the need for a H2 acceptor, offering an efficient and selective protocol for the synthesis of a new family of heterocyclic [1,3]-thiasilolanes.\",\"PeriodicalId\":67,\"journal\":{\"name\":\"Chemical Communications\",\"volume\":\"115 1\",\"pages\":\"\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2025-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Communications\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1039/d5cc04330a\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Communications","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5cc04330a","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

摘要

利用半夹心稀土催化剂首次实现了烷基硫化物与氢硅烷的α-C(sp3)-H硅化反应。这种转化过程顺利进行,不需要H2受体,为合成新的杂环[1,3]-噻唑硅烷家族提供了一种高效和选择性的方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis of [1,3]-thiasilolanes via rare-earth-catalysed intramolecular α-C(sp3)-H silylation of alkyl sulphides with hydrosilanes
The intramolecular α-C(sp3)-H silylation of alkyl sulfides with hydrosilanes has been achieved for the first time by the use of halfsandwich rare-earth catalysts. This transformation smoothly proceeds without the need for a H2 acceptor, offering an efficient and selective protocol for the synthesis of a new family of heterocyclic [1,3]-thiasilolanes.
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
Chemical Communications
Chemical Communications 化学-化学综合
CiteScore
8.60
自引率
4.10%
发文量
2705
审稿时长
1.4 months
期刊介绍: ChemComm (Chemical Communications) is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world''s major areas of chemical research.
×
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