{"title":"电化学脱羧磺化:一种温和有效的获取有机硫酸盐的方法","authors":"Wei Sheng, Huanhuan Peng, Chunlan Song, Jiakun Li","doi":"10.1021/acs.joc.5c00504","DOIUrl":null,"url":null,"abstract":"Sulfation is a crucial transformation in both pathological and physiological processes. However, the conventional synthesis of organosulfates primarily relies on <i>O</i>-sulfonation, which is limited to hydroxyl-containing substrates. Here, we developed a practical and cost-efficient method for electrochemical decarboxylative sulfation. This approach opens new avenues to access organosulfates from readily available carboxylic acids with a broad substrate scope and good functional group compatibility.","PeriodicalId":57,"journal":{"name":"Journal of Organic Chemistry","volume":"9 1","pages":""},"PeriodicalIF":3.6000,"publicationDate":"2025-06-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Electrochemical Decarboxylative Sulfation: A Mild and Efficient Method to Access Organosulfates\",\"authors\":\"Wei Sheng, Huanhuan Peng, Chunlan Song, Jiakun Li\",\"doi\":\"10.1021/acs.joc.5c00504\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Sulfation is a crucial transformation in both pathological and physiological processes. However, the conventional synthesis of organosulfates primarily relies on <i>O</i>-sulfonation, which is limited to hydroxyl-containing substrates. Here, we developed a practical and cost-efficient method for electrochemical decarboxylative sulfation. This approach opens new avenues to access organosulfates from readily available carboxylic acids with a broad substrate scope and good functional group compatibility.\",\"PeriodicalId\":57,\"journal\":{\"name\":\"Journal of Organic Chemistry\",\"volume\":\"9 1\",\"pages\":\"\"},\"PeriodicalIF\":3.6000,\"publicationDate\":\"2025-06-04\",\"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.5c00504\",\"RegionNum\":2,\"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":"Journal of Organic Chemistry","FirstCategoryId":"1","ListUrlMain":"https://doi.org/10.1021/acs.joc.5c00504","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Electrochemical Decarboxylative Sulfation: A Mild and Efficient Method to Access Organosulfates
Sulfation is a crucial transformation in both pathological and physiological processes. However, the conventional synthesis of organosulfates primarily relies on O-sulfonation, which is limited to hydroxyl-containing substrates. Here, we developed a practical and cost-efficient method for electrochemical decarboxylative sulfation. This approach opens new avenues to access organosulfates from readily available carboxylic acids with a broad substrate scope and good functional group compatibility.
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.