{"title":"One-Pot Synthesis of Benzoxazoles and Sulfoxides: Complete Utilization of Diaryl Sulfoxides","authors":"Chuntao Zhong, Guangcai Qu, Jingdi Wang, Baoshan Xu, Benqiang Cui, Yanhui Shi, Changsheng Cao","doi":"10.1021/acs.joc.5c00274","DOIUrl":null,"url":null,"abstract":"Synthesis of 2-aryl benzoxazoles and aryl sulfoxide derivatives in a one-pot process has been developed via the palladium-catalyzed cross-coupling of diaryl sulfoxides with benzoxazoles, followed by trapping the remaining sulfenate anions with different electrophilic reagents. The reaction involves the C–S and C–H bond activation and the C–C and C–S bond formation. The protocol allows a broad scope of substrates, functional group tolerance, and scalability.","PeriodicalId":57,"journal":{"name":"Journal of Organic Chemistry","volume":"44 1","pages":""},"PeriodicalIF":3.3000,"publicationDate":"2025-04-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Organic Chemistry","FirstCategoryId":"1","ListUrlMain":"https://doi.org/10.1021/acs.joc.5c00274","RegionNum":2,"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
Synthesis of 2-aryl benzoxazoles and aryl sulfoxide derivatives in a one-pot process has been developed via the palladium-catalyzed cross-coupling of diaryl sulfoxides with benzoxazoles, followed by trapping the remaining sulfenate anions with different electrophilic reagents. The reaction involves the C–S and C–H bond activation and the C–C and C–S bond formation. The protocol allows a broad scope of substrates, functional group tolerance, and scalability.
期刊介绍:
Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.