铁催化的结构不同的 Si- 卤代二烯烃的 γ-多卤烷基化反应

Justin, Mohr, Douglas, Yarbrough, Brian, Osei-Badu, Cole, Wagner, Kayla, Storme, Sebastian, Marquez R.
{"title":"铁催化的结构不同的 Si- 卤代二烯烃的 γ-多卤烷基化反应","authors":"Justin, Mohr, Douglas, Yarbrough, Brian, Osei-Badu, Cole, Wagner, Kayla, Storme, Sebastian, Marquez R.","doi":"10.26434/chemrxiv-2024-78vqn","DOIUrl":null,"url":null,"abstract":"Regioselective γ-polyhaloalkylation is achieved using tetrahalomethanes or α,α,α-trihaloalkyl compounds and siloxydienes via Fe(II) catalysis. A range of siloxydienes are functionalized in good yield and high stereoselectivity under mild reaction conditions. Structural divergence is observed as either haloalkylated or haloalkenylated products are formed based on substitution pattern of the siloxydiene. The halogenated products show utility in further synthetic transformations selec- tive reduction and cross coupling reactions.","PeriodicalId":9813,"journal":{"name":"ChemRxiv","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Fe-Catalyzed Structurally Divergent γ-Polyhaloalkylation of Si- loxydienes\",\"authors\":\"Justin, Mohr, Douglas, Yarbrough, Brian, Osei-Badu, Cole, Wagner, Kayla, Storme, Sebastian, Marquez R.\",\"doi\":\"10.26434/chemrxiv-2024-78vqn\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Regioselective γ-polyhaloalkylation is achieved using tetrahalomethanes or α,α,α-trihaloalkyl compounds and siloxydienes via Fe(II) catalysis. A range of siloxydienes are functionalized in good yield and high stereoselectivity under mild reaction conditions. Structural divergence is observed as either haloalkylated or haloalkenylated products are formed based on substitution pattern of the siloxydiene. The halogenated products show utility in further synthetic transformations selec- tive reduction and cross coupling reactions.\",\"PeriodicalId\":9813,\"journal\":{\"name\":\"ChemRxiv\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-09-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ChemRxiv\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.26434/chemrxiv-2024-78vqn\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemRxiv","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.26434/chemrxiv-2024-78vqn","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

利用四卤甲烷或 α,α,α-三卤烷基化合物和硅氧烷,通过 Fe(II) 催化实现了区域选择性 γ-多卤烷基化。在温和的反应条件下,一系列硅氧二烯烃以良好的收率和较高的立体选择性实现了官能化。根据硅氧烷的取代模式,可以观察到卤代烃化或卤代烯化产物的结构差异。卤化产物可用于进一步的合成转化、选择性还原和交叉偶联反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fe-Catalyzed Structurally Divergent γ-Polyhaloalkylation of Si- loxydienes
Regioselective γ-polyhaloalkylation is achieved using tetrahalomethanes or α,α,α-trihaloalkyl compounds and siloxydienes via Fe(II) catalysis. A range of siloxydienes are functionalized in good yield and high stereoselectivity under mild reaction conditions. Structural divergence is observed as either haloalkylated or haloalkenylated products are formed based on substitution pattern of the siloxydiene. The halogenated products show utility in further synthetic transformations selec- tive reduction and cross coupling reactions.
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
自引率
0.00%
发文量
0
×
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