E. Koneva, E. V. Suslov, D. Korchagina, A. Genaev, K. Volcho, N. Salakhutdinov
{"title":"用α-蒎烯衍生配体催化二乙基锌与苯甲醛的不对称加成","authors":"E. Koneva, E. V. Suslov, D. Korchagina, A. Genaev, K. Volcho, N. Salakhutdinov","doi":"10.2174/1876214X01104010107","DOIUrl":null,"url":null,"abstract":"The amines obtained from � -pinene and containing a phenol or pyridine fragment can be used as ligands in the asymmetric addition of diethylzinc to aromatic aldehydes; the enantiomeric excess (ee) was up to 80%. The enantioselectivity of the reaction is not very sensitive to the nature of substituents in the aromatic ring of aldehydes.","PeriodicalId":22755,"journal":{"name":"The Open Catalysis Journal","volume":"32 1","pages":"107-112"},"PeriodicalIF":0.0000,"publicationDate":"2011-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"7","resultStr":"{\"title\":\"Catalytic Asymmetric Addition of Diethylzinc to Benzaldehyde Using α- Pinene-Derived Ligands\",\"authors\":\"E. Koneva, E. V. Suslov, D. Korchagina, A. Genaev, K. Volcho, N. Salakhutdinov\",\"doi\":\"10.2174/1876214X01104010107\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The amines obtained from � -pinene and containing a phenol or pyridine fragment can be used as ligands in the asymmetric addition of diethylzinc to aromatic aldehydes; the enantiomeric excess (ee) was up to 80%. The enantioselectivity of the reaction is not very sensitive to the nature of substituents in the aromatic ring of aldehydes.\",\"PeriodicalId\":22755,\"journal\":{\"name\":\"The Open Catalysis Journal\",\"volume\":\"32 1\",\"pages\":\"107-112\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2011-09-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"7\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Open Catalysis Journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2174/1876214X01104010107\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Open Catalysis Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/1876214X01104010107","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Catalytic Asymmetric Addition of Diethylzinc to Benzaldehyde Using α- Pinene-Derived Ligands
The amines obtained from � -pinene and containing a phenol or pyridine fragment can be used as ligands in the asymmetric addition of diethylzinc to aromatic aldehydes; the enantiomeric excess (ee) was up to 80%. The enantioselectivity of the reaction is not very sensitive to the nature of substituents in the aromatic ring of aldehydes.