{"title":"1、2、3-Benzothiadiazoles。第五部分:7-氨基苯并异噻唑类重氮盐的重排","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":"{\"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}","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}
1,2,3-Benzothiadiazoles. Part V. The rearrangement of diazonium salts derived from 7-aminobenzisothiazoles
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.
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