{"title":"K2CO3/ tfaa活化α-磺酰基邻羟基苯乙酮与邻硝基二硫化物的二酰化反应生成磺酰基双邻硝基苯乙酮†","authors":"Meng-Yang Chang , Nai-Chen Hsueh","doi":"10.1039/d5ob00380f","DOIUrl":null,"url":null,"abstract":"<div><div>A concise K<sub>2</sub>CO<sub>3</sub>/TFAA-mediated diarylation of readily accessible sulfonyl <em>o</em>-hydroxyacetophenones with <em>o</em>-nitroaryl disulfides is described. This single-step strategy provides a variety of functionalized sulfonyl <em>C</em>- and <em>O</em>-bis-<em>o</em>-nitroaryl acetophenones <em>via</em> the formation of one carbon–carbon single bond and one carbon–oxygen single bond. A plausible mechanism is proposed and discussed. The molecular structures of key products were determined by X-ray analysis.</div></div>","PeriodicalId":96,"journal":{"name":"Organic & Biomolecular Chemistry","volume":"23 19","pages":"Pages 4751-4757"},"PeriodicalIF":2.7000,"publicationDate":"2025-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"K2CO3/TFAA-activated diarylation of α-sulfonyl o-hydroxyacetophenones with o-nitroaryl disulfides to construct sulfonyl bis-o-nitroaryl acetophenones†\",\"authors\":\"Meng-Yang Chang , Nai-Chen Hsueh\",\"doi\":\"10.1039/d5ob00380f\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>A concise K<sub>2</sub>CO<sub>3</sub>/TFAA-mediated diarylation of readily accessible sulfonyl <em>o</em>-hydroxyacetophenones with <em>o</em>-nitroaryl disulfides is described. This single-step strategy provides a variety of functionalized sulfonyl <em>C</em>- and <em>O</em>-bis-<em>o</em>-nitroaryl acetophenones <em>via</em> the formation of one carbon–carbon single bond and one carbon–oxygen single bond. A plausible mechanism is proposed and discussed. The molecular structures of key products were determined by X-ray analysis.</div></div>\",\"PeriodicalId\":96,\"journal\":{\"name\":\"Organic & Biomolecular Chemistry\",\"volume\":\"23 19\",\"pages\":\"Pages 4751-4757\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2025-04-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic & Biomolecular Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S1477052025003222\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic & Biomolecular Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1477052025003222","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
K2CO3/TFAA-activated diarylation of α-sulfonyl o-hydroxyacetophenones with o-nitroaryl disulfides to construct sulfonyl bis-o-nitroaryl acetophenones†
A concise K2CO3/TFAA-mediated diarylation of readily accessible sulfonyl o-hydroxyacetophenones with o-nitroaryl disulfides is described. This single-step strategy provides a variety of functionalized sulfonyl C- and O-bis-o-nitroaryl acetophenones via the formation of one carbon–carbon single bond and one carbon–oxygen single bond. A plausible mechanism is proposed and discussed. The molecular structures of key products were determined by X-ray analysis.
期刊介绍:
Organic & Biomolecular Chemistry is an international journal using integrated research in chemistry-organic chemistry. Founded in 2003 by the Royal Society of Chemistry, the journal is published in Semimonthly issues and has been indexed by SCIE, a leading international database. The journal focuses on the key research and cutting-edge progress in the field of chemistry-organic chemistry, publishes and reports the research results in this field in a timely manner, and is committed to becoming a window and platform for rapid academic exchanges among peers in this field. The journal's impact factor in 2023 is 2.9, and its CiteScore is 5.5.