{"title":"5,13-二乙基-10-甲基-8-庚烷酮:1976年后kelelex 100的组分","authors":"H. Striegel, W. Wiegrebe","doi":"10.1135/CCCC19912203","DOIUrl":null,"url":null,"abstract":"The title compound was prepared by mixed aldol condensation of 2-ethylhexanal and acetone, double bond hydrogenation, aldol autocondensation of the resulting saturated ketone and finel double bond hydrogenation. It is identical with the ketone C 22 H 44 O previously isolated from new Kelex 100 which was erroneously assigned a furoquinoline structure.","PeriodicalId":10674,"journal":{"name":"Collection of Czechoslovak Chemical Communications","volume":"56 1","pages":"2203-2208"},"PeriodicalIF":0.0000,"publicationDate":"1991-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":"{\"title\":\"5,13-Diethyl-10-methyl-8-heptadecanone: A Component of Post - 1976 Kelex 100\",\"authors\":\"H. Striegel, W. Wiegrebe\",\"doi\":\"10.1135/CCCC19912203\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The title compound was prepared by mixed aldol condensation of 2-ethylhexanal and acetone, double bond hydrogenation, aldol autocondensation of the resulting saturated ketone and finel double bond hydrogenation. It is identical with the ketone C 22 H 44 O previously isolated from new Kelex 100 which was erroneously assigned a furoquinoline structure.\",\"PeriodicalId\":10674,\"journal\":{\"name\":\"Collection of Czechoslovak Chemical Communications\",\"volume\":\"56 1\",\"pages\":\"2203-2208\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1991-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Collection of Czechoslovak Chemical Communications\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1135/CCCC19912203\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Collection of Czechoslovak Chemical Communications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1135/CCCC19912203","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
5,13-Diethyl-10-methyl-8-heptadecanone: A Component of Post - 1976 Kelex 100
The title compound was prepared by mixed aldol condensation of 2-ethylhexanal and acetone, double bond hydrogenation, aldol autocondensation of the resulting saturated ketone and finel double bond hydrogenation. It is identical with the ketone C 22 H 44 O previously isolated from new Kelex 100 which was erroneously assigned a furoquinoline structure.
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