通过协同催化选择性 C-C 键裂解和随后的烯烃底物 Silylperoxylation 来延长碳链

IF 11.3 1区 化学 Q1 CHEMISTRY, PHYSICAL ACS Catalysis Pub Date : 2024-09-20 DOI:10.1021/acscatal.4c04886
Jia-Hao Xie, Terumasa Kato, Keiji Maruoka
{"title":"通过协同催化选择性 C-C 键裂解和随后的烯烃底物 Silylperoxylation 来延长碳链","authors":"Jia-Hao Xie, Terumasa Kato, Keiji Maruoka","doi":"10.1021/acscatal.4c04886","DOIUrl":null,"url":null,"abstract":"A Co-catalyzed selective C–C bond cleavage followed by the silylperoxylation of alkene substrates generated a series of alkylsilyl peroxides with good yields and selectivities. Further transformation through transition-metal-catalyzed cleavage of the resulting alkylsilyl peroxides and subsequent functionalization with coupling partners could generate a series of dicarbonyl compounds. This two-step transformation was carried out in a one-pot manner, which enhances the practicability of this approach. A plausible reaction mechanism was proposed to interpret the C–C bond cleavage and subsequent silylperoxylation of the alkene substrates.","PeriodicalId":9,"journal":{"name":"ACS Catalysis ","volume":null,"pages":null},"PeriodicalIF":11.3000,"publicationDate":"2024-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Carbon-Chain Elongation by Co-Catalyzed Selective C–C Bond Cleavage and Subsequent Silylperoxylation of Alkene Substrates\",\"authors\":\"Jia-Hao Xie, Terumasa Kato, Keiji Maruoka\",\"doi\":\"10.1021/acscatal.4c04886\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A Co-catalyzed selective C–C bond cleavage followed by the silylperoxylation of alkene substrates generated a series of alkylsilyl peroxides with good yields and selectivities. Further transformation through transition-metal-catalyzed cleavage of the resulting alkylsilyl peroxides and subsequent functionalization with coupling partners could generate a series of dicarbonyl compounds. This two-step transformation was carried out in a one-pot manner, which enhances the practicability of this approach. A plausible reaction mechanism was proposed to interpret the C–C bond cleavage and subsequent silylperoxylation of the alkene substrates.\",\"PeriodicalId\":9,\"journal\":{\"name\":\"ACS Catalysis \",\"volume\":null,\"pages\":null},\"PeriodicalIF\":11.3000,\"publicationDate\":\"2024-09-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Catalysis \",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/acscatal.4c04886\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Catalysis ","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acscatal.4c04886","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

摘要

通过共催化选择性 C-C 键裂解,然后对烯烃底物进行硅烷过氧化反应,生成了一系列烷基硅基过氧化物,而且产量和选择性都很好。通过过渡金属催化裂解生成的烷基硅基过氧化物并随后与偶联剂官能化,可进一步转化生成一系列二羰基化合物。这种两步转化以一锅方式进行,提高了这种方法的实用性。为了解释烯烃底物的 C-C 键裂解和随后的硅基过氧化反应,提出了一种合理的反应机理。
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
Carbon-Chain Elongation by Co-Catalyzed Selective C–C Bond Cleavage and Subsequent Silylperoxylation of Alkene Substrates
A Co-catalyzed selective C–C bond cleavage followed by the silylperoxylation of alkene substrates generated a series of alkylsilyl peroxides with good yields and selectivities. Further transformation through transition-metal-catalyzed cleavage of the resulting alkylsilyl peroxides and subsequent functionalization with coupling partners could generate a series of dicarbonyl compounds. This two-step transformation was carried out in a one-pot manner, which enhances the practicability of this approach. A plausible reaction mechanism was proposed to interpret the C–C bond cleavage and subsequent silylperoxylation of the alkene substrates.
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
ACS Catalysis
ACS Catalysis CHEMISTRY, PHYSICAL-
CiteScore
20.80
自引率
6.20%
发文量
1253
审稿时长
1.5 months
期刊介绍: ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels. The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.
期刊最新文献
Dendrite-free zinc metal anode for long-life zinc-ion batteries enabled by an artificial hydrophobic-zincophilic coating. Bioderived carbon aerogels loaded with g-C3N4 and their high Efficacy removing volatile organic compounds (VOCs). Crosslinking modification of starch improves the structural stability of hard carbon anodes for high-capacity sodium storage. Interfacial design of pyrene-based covalent organic framework for overall photocatalytic H2O2 synthesis in water. LaCo0.95Mo0.05O3/CeO2 composite can promote the effective activation of peroxymonosulfate via Co3+/Co2+ cycle and realize the efficient degradation of hydroxychloroquine sulfate.
×
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学术文献互助
Book学术文献互助群
群 号:481959085
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