{"title":"Azonia-azulene盐。第四部分:将二氢吲哚嘧啶转化为偶氮-偶氮烯的尝试","authors":"G. Cliff, Gurnos Jones, J. Stanyer","doi":"10.1039/J39710003426","DOIUrl":null,"url":null,"abstract":"The reduction of indolizine (1) and of some substituted indolizines [(6), (8), (10), and (13)] by dissolving metals gave 5,6- and 5,8-dihydroindolizines and 5,6,7,8-tetrahydroindolizines. Attempts to add carbenes to the 5,6-dihydro-2-phenylindolizines (7) and (9) were unsuccessful.","PeriodicalId":17245,"journal":{"name":"Journal of The Chemical Society C: Organic","volume":"16 1","pages":"3426-3427"},"PeriodicalIF":0.0000,"publicationDate":"1971-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"5","resultStr":"{\"title\":\"Azonia-azulene salts. Part IV. Attempts to convert dihydroindolizines into azonia-azulenes\",\"authors\":\"G. Cliff, Gurnos Jones, J. Stanyer\",\"doi\":\"10.1039/J39710003426\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The reduction of indolizine (1) and of some substituted indolizines [(6), (8), (10), and (13)] by dissolving metals gave 5,6- and 5,8-dihydroindolizines and 5,6,7,8-tetrahydroindolizines. Attempts to add carbenes to the 5,6-dihydro-2-phenylindolizines (7) and (9) were unsuccessful.\",\"PeriodicalId\":17245,\"journal\":{\"name\":\"Journal of The Chemical Society C: Organic\",\"volume\":\"16 1\",\"pages\":\"3426-3427\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1971-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"5\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of The Chemical Society C: Organic\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1039/J39710003426\",\"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/J39710003426","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Azonia-azulene salts. Part IV. Attempts to convert dihydroindolizines into azonia-azulenes
The reduction of indolizine (1) and of some substituted indolizines [(6), (8), (10), and (13)] by dissolving metals gave 5,6- and 5,8-dihydroindolizines and 5,6,7,8-tetrahydroindolizines. Attempts to add carbenes to the 5,6-dihydro-2-phenylindolizines (7) and (9) were unsuccessful.
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