{"title":"共轭不饱和酮。Wohl-Ziegler反应","authors":"Ping-Yuan Yeh","doi":"10.1002/jccs.195400010","DOIUrl":null,"url":null,"abstract":"<p>The structures of the products resulting from the reactions of N-bromosuccinimide with dibenzalcyclohexanon and with dibenzalcyclo-Pentanons, as well as their tetrabromides, were established. The ethylenic linkage remaining in the tetrabromides did not add bromine, while they were catalytically hydrogenated to give the corresponding cycloalkanone derivatives.</p>","PeriodicalId":73978,"journal":{"name":"","volume":"1 1","pages":"106-112"},"PeriodicalIF":0.0,"publicationDate":"1954-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/jccs.195400010","citationCount":"4","resultStr":"{\"title\":\"Conjugated Unsaturated Ketones. IV. The Wohl-Ziegler Reaction\",\"authors\":\"Ping-Yuan Yeh\",\"doi\":\"10.1002/jccs.195400010\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>The structures of the products resulting from the reactions of N-bromosuccinimide with dibenzalcyclohexanon and with dibenzalcyclo-Pentanons, as well as their tetrabromides, were established. The ethylenic linkage remaining in the tetrabromides did not add bromine, while they were catalytically hydrogenated to give the corresponding cycloalkanone derivatives.</p>\",\"PeriodicalId\":73978,\"journal\":{\"name\":\"\",\"volume\":\"1 1\",\"pages\":\"106-112\"},\"PeriodicalIF\":0.0,\"publicationDate\":\"1954-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1002/jccs.195400010\",\"citationCount\":\"4\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/jccs.195400010\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/jccs.195400010","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Conjugated Unsaturated Ketones. IV. The Wohl-Ziegler Reaction
The structures of the products resulting from the reactions of N-bromosuccinimide with dibenzalcyclohexanon and with dibenzalcyclo-Pentanons, as well as their tetrabromides, were established. The ethylenic linkage remaining in the tetrabromides did not add bromine, while they were catalytically hydrogenated to give the corresponding cycloalkanone derivatives.
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