{"title":"卤化桥接多环化合物的自由基反应。十三。溴化氢加成六氯甲基冰片烯","authors":"R. Alexander, D. I. Davies","doi":"10.1039/J39710000896","DOIUrl":null,"url":null,"abstract":"The free-radical addition of hydrogen bromide to hexachloromethylenenorbornene affords a 60 : 40 mixture of 1-bromomethyl-2,3,4,5,5,6-endo-hexachloronorborn-2-ene and 5-endo-bromomethyl-1,2,3,4,7,7-hexachloronorborn-2-ene. The aluminium bromide-catalysed ionic addition gives a 68 : 32 mixture of 5-exo-bromo-1,2,3,4,7,7-hexachloro-5-endo-methylnorborn-2-ene and its 5-endo-bromo-epimer.","PeriodicalId":17245,"journal":{"name":"Journal of The Chemical Society C: Organic","volume":"4 1","pages":"896-898"},"PeriodicalIF":0.0000,"publicationDate":"1971-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Free-radical reactions of halogenated bridged polycyclic compounds. Part XIII. The addition of hydrogen bromide to hexachloromethylenenorbornene\",\"authors\":\"R. Alexander, D. I. Davies\",\"doi\":\"10.1039/J39710000896\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The free-radical addition of hydrogen bromide to hexachloromethylenenorbornene affords a 60 : 40 mixture of 1-bromomethyl-2,3,4,5,5,6-endo-hexachloronorborn-2-ene and 5-endo-bromomethyl-1,2,3,4,7,7-hexachloronorborn-2-ene. The aluminium bromide-catalysed ionic addition gives a 68 : 32 mixture of 5-exo-bromo-1,2,3,4,7,7-hexachloro-5-endo-methylnorborn-2-ene and its 5-endo-bromo-epimer.\",\"PeriodicalId\":17245,\"journal\":{\"name\":\"Journal of The Chemical Society C: Organic\",\"volume\":\"4 1\",\"pages\":\"896-898\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1971-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of The Chemical Society C: Organic\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1039/J39710000896\",\"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/J39710000896","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Free-radical reactions of halogenated bridged polycyclic compounds. Part XIII. The addition of hydrogen bromide to hexachloromethylenenorbornene
The free-radical addition of hydrogen bromide to hexachloromethylenenorbornene affords a 60 : 40 mixture of 1-bromomethyl-2,3,4,5,5,6-endo-hexachloronorborn-2-ene and 5-endo-bromomethyl-1,2,3,4,7,7-hexachloronorborn-2-ene. The aluminium bromide-catalysed ionic addition gives a 68 : 32 mixture of 5-exo-bromo-1,2,3,4,7,7-hexachloro-5-endo-methylnorborn-2-ene and its 5-endo-bromo-epimer.
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