{"title":"电化学催化的 Rh 催化苯甲酸与炔基酯/酰胺的区域选择性 [4 + 1] 和 [4 + 2] 环加成反应†‡","authors":"Wei-Jung Chiu and Chung-Ming Sun","doi":"10.1039/D4GC03753G","DOIUrl":null,"url":null,"abstract":"<p >A Rh(<small>III</small>)-catalyzed additive-controlled regioselective [4 + 1] and [4 + 2] cyclization of benzoic acids with alkynyl esters/amides under electrochemical conditions has been developed for the synthesis of phthalides and isocoumarins. The selectivity for the product formation was attained by merely changing the additive. Employment of NaOAc in the reaction produces isocoumarins whereas AcOH favors phthalides. Cyclic voltammetry and control experiments reveal the mechanistic pathway of the reaction.</p>","PeriodicalId":9,"journal":{"name":"ACS Catalysis ","volume":null,"pages":null},"PeriodicalIF":11.3000,"publicationDate":"2024-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Electrochemistry-enabled Rh-catalyzed regioselective [4 + 1] and [4 + 2] cycloaddition of benzoic acid with alkynyl esters/amides†‡\",\"authors\":\"Wei-Jung Chiu and Chung-Ming Sun\",\"doi\":\"10.1039/D4GC03753G\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >A Rh(<small>III</small>)-catalyzed additive-controlled regioselective [4 + 1] and [4 + 2] cyclization of benzoic acids with alkynyl esters/amides under electrochemical conditions has been developed for the synthesis of phthalides and isocoumarins. The selectivity for the product formation was attained by merely changing the additive. Employment of NaOAc in the reaction produces isocoumarins whereas AcOH favors phthalides. Cyclic voltammetry and control experiments reveal the mechanistic pathway of the reaction.</p>\",\"PeriodicalId\":9,\"journal\":{\"name\":\"ACS Catalysis \",\"volume\":null,\"pages\":null},\"PeriodicalIF\":11.3000,\"publicationDate\":\"2024-10-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Catalysis \",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2024/gc/d4gc03753g\",\"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://pubs.rsc.org/en/content/articlelanding/2024/gc/d4gc03753g","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Electrochemistry-enabled Rh-catalyzed regioselective [4 + 1] and [4 + 2] cycloaddition of benzoic acid with alkynyl esters/amides†‡
A Rh(III)-catalyzed additive-controlled regioselective [4 + 1] and [4 + 2] cyclization of benzoic acids with alkynyl esters/amides under electrochemical conditions has been developed for the synthesis of phthalides and isocoumarins. The selectivity for the product formation was attained by merely changing the additive. Employment of NaOAc in the reaction produces isocoumarins whereas AcOH favors phthalides. Cyclic voltammetry and control experiments reveal the mechanistic pathway of the reaction.
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.