Yu Wang , Hongkun Huang , Xueyu Fang , Chun Ling , Tian Chen , Hua Yao , Zhaohua Yan
{"title":"DTBP/HCl介导咪唑吡啶与亚磺酸的磺化反应","authors":"Yu Wang , Hongkun Huang , Xueyu Fang , Chun Ling , Tian Chen , Hua Yao , Zhaohua Yan","doi":"10.1016/j.rechem.2025.102428","DOIUrl":null,"url":null,"abstract":"<div><div>A direct sulfenylation reaction of imidazopyridines with sulfinic acid mediated by di-<em>tert</em>-butylperoxide (DTBP) and hydrochloric acid was developed leading to the introduction of C<img>S bonds into the imidazo[1,2-<em>a</em>]pyridine skeleton. The reaction proceeded under transition-metal-free conditions with good functional group tolerance and moderate to excellent yields.</div></div>","PeriodicalId":420,"journal":{"name":"Results in Chemistry","volume":"16 ","pages":"Article 102428"},"PeriodicalIF":2.5000,"publicationDate":"2025-06-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The sulfenylation of imidazopyridines with sulfinic acids mediated by DTBP/HCl\",\"authors\":\"Yu Wang , Hongkun Huang , Xueyu Fang , Chun Ling , Tian Chen , Hua Yao , Zhaohua Yan\",\"doi\":\"10.1016/j.rechem.2025.102428\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>A direct sulfenylation reaction of imidazopyridines with sulfinic acid mediated by di-<em>tert</em>-butylperoxide (DTBP) and hydrochloric acid was developed leading to the introduction of C<img>S bonds into the imidazo[1,2-<em>a</em>]pyridine skeleton. The reaction proceeded under transition-metal-free conditions with good functional group tolerance and moderate to excellent yields.</div></div>\",\"PeriodicalId\":420,\"journal\":{\"name\":\"Results in Chemistry\",\"volume\":\"16 \",\"pages\":\"Article 102428\"},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2025-06-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Results in Chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2211715625004114\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Results in Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2211715625004114","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
The sulfenylation of imidazopyridines with sulfinic acids mediated by DTBP/HCl
A direct sulfenylation reaction of imidazopyridines with sulfinic acid mediated by di-tert-butylperoxide (DTBP) and hydrochloric acid was developed leading to the introduction of CS bonds into the imidazo[1,2-a]pyridine skeleton. The reaction proceeded under transition-metal-free conditions with good functional group tolerance and moderate to excellent yields.