{"title":"通过氢化铁氢原子转移实现还原性烯烃双环[1.1.0]丁烷偶联","authors":"Guang Chen, Dayu Tian, Xiaocheng Wang, Hai-Jun Zhang","doi":"10.1021/acscatal.4c04837","DOIUrl":null,"url":null,"abstract":"Here, we present the reductive olefin bicyclo[1.1.0]butane coupling method enabled by iron hydride hydrogen atom transfer. Thus, readily available olefins can serve as competent C(sp<sup>3</sup>)-centered radical precursors, reacting with bicyclo[1.1.0]butanes under an ambient atmosphere to deliver valuable alkylated cyclobutanes. More than 40 examples are presented with a wide range of substrates, demonstrating the mildness of this operationally simple protocol. Most importantly, this method allows the rapid synthesis of cyclobutane analogues for bioactive compounds that would otherwise be difficult to access.","PeriodicalId":9,"journal":{"name":"ACS Catalysis ","volume":null,"pages":null},"PeriodicalIF":11.3000,"publicationDate":"2024-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Reductive Olefin Bicyclo[1.1.0]butane Coupling Enabled by Iron Hydride Hydrogen Atom Transfer\",\"authors\":\"Guang Chen, Dayu Tian, Xiaocheng Wang, Hai-Jun Zhang\",\"doi\":\"10.1021/acscatal.4c04837\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Here, we present the reductive olefin bicyclo[1.1.0]butane coupling method enabled by iron hydride hydrogen atom transfer. Thus, readily available olefins can serve as competent C(sp<sup>3</sup>)-centered radical precursors, reacting with bicyclo[1.1.0]butanes under an ambient atmosphere to deliver valuable alkylated cyclobutanes. More than 40 examples are presented with a wide range of substrates, demonstrating the mildness of this operationally simple protocol. Most importantly, this method allows the rapid synthesis of cyclobutane analogues for bioactive compounds that would otherwise be difficult to access.\",\"PeriodicalId\":9,\"journal\":{\"name\":\"ACS Catalysis \",\"volume\":null,\"pages\":null},\"PeriodicalIF\":11.3000,\"publicationDate\":\"2024-09-25\",\"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.4c04837\",\"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.4c04837","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Reductive Olefin Bicyclo[1.1.0]butane Coupling Enabled by Iron Hydride Hydrogen Atom Transfer
Here, we present the reductive olefin bicyclo[1.1.0]butane coupling method enabled by iron hydride hydrogen atom transfer. Thus, readily available olefins can serve as competent C(sp3)-centered radical precursors, reacting with bicyclo[1.1.0]butanes under an ambient atmosphere to deliver valuable alkylated cyclobutanes. More than 40 examples are presented with a wide range of substrates, demonstrating the mildness of this operationally simple protocol. Most importantly, this method allows the rapid synthesis of cyclobutane analogues for bioactive compounds that would otherwise be difficult to access.
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.