{"title":"1,2,3-Benzothiadiazoles. Part V. The rearrangement of diazonium salts derived from 7-aminobenzisothiazoles","authors":"E. Haddock, P. Kirby, A. Johnson","doi":"10.1039/J39710003994","DOIUrl":null,"url":null,"abstract":"The rearrangement of benzisothiazole-7-diazonium salts to 7-acylbenzothiadiazoles is favoured over the standard reactions involving elimination of nitrogen by the presence of certain metal salts; the extent of these two competing reactions is governed by the oxidation potential of the metal.","PeriodicalId":17245,"journal":{"name":"Journal of The Chemical Society C: Organic","volume":"20 1","pages":"3994-3999"},"PeriodicalIF":0.0000,"publicationDate":"1971-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"11","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of The Chemical Society C: Organic","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1039/J39710003994","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 11
Abstract
The rearrangement of benzisothiazole-7-diazonium salts to 7-acylbenzothiadiazoles is favoured over the standard reactions involving elimination of nitrogen by the presence of certain metal salts; the extent of these two competing reactions is governed by the oxidation potential of the metal.