Synthesis of alkyl sulfones via a photocatalytic multicomponent reaction of aryldiazo tetrafluoroborate salts, styrene derivatives, and sodium metabisulfite.
{"title":"Synthesis of alkyl sulfones <i>via</i> a photocatalytic multicomponent reaction of aryldiazo tetrafluoroborate salts, styrene derivatives, and sodium metabisulfite.","authors":"Truong Giang Luu, Hee-Kwon Kim","doi":"10.1039/d4ob01664e","DOIUrl":null,"url":null,"abstract":"<p><p>Alkyl sulfones are found in numerous valuable organic molecules. Here, we describe a promising approach for the one-pot synthesis of alkyl sulfones under visible light. Aryl diazo salts were allowed to react with styrene derivatives and sodium metabisulfite in the presence of thiophenol as a hydrogen atom transfer reagent and rhodamine B as a photocatalyst to yield alkyl sulfones. Using this process, various alkyl sulfones were readily synthesized under mild reaction conditions. Our results suggest that this approach can provide diverse and valuable sulfones.</p>","PeriodicalId":96,"journal":{"name":"Organic & Biomolecular Chemistry","volume":" ","pages":""},"PeriodicalIF":2.9000,"publicationDate":"2024-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic & Biomolecular Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d4ob01664e","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0
Abstract
Alkyl sulfones are found in numerous valuable organic molecules. Here, we describe a promising approach for the one-pot synthesis of alkyl sulfones under visible light. Aryl diazo salts were allowed to react with styrene derivatives and sodium metabisulfite in the presence of thiophenol as a hydrogen atom transfer reagent and rhodamine B as a photocatalyst to yield alkyl sulfones. Using this process, various alkyl sulfones were readily synthesized under mild reaction conditions. Our results suggest that this approach can provide diverse and valuable sulfones.