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A New Convenient Method for the Resolution of 1, 1'-Binaphthalene-2, 2'-diol Via a Phosphite Using (-)-Menthol as Resolving Agent
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作者 JueXiaoCAI ChihuangYEUNG 《Chinese Chemical Letters》 SCIE CAS CSCD 2002年第7期617-619,共3页
Menthol reacts with phosphorus trichloride to afford menthyl phosphorodichloridite 2, which further reacts with racemic 1, 1-binaphthalene-2, 2-diol to give phosphite (+)-3 in the presence of triethylamine. (+)-3 can ... Menthol reacts with phosphorus trichloride to afford menthyl phosphorodichloridite 2, which further reacts with racemic 1, 1-binaphthalene-2, 2-diol to give phosphite (+)-3 in the presence of triethylamine. (+)-3 can be easily separated by fractional crystallization to form the crystal (+)-(S)-3 and the mother liquor (-)-(R)-3. Then both the crystal and the mother liquor are treated with AcOH-H2O to obtain enantiomeric pure (-)-(S)-1 and (+)-(R)-1 respectively, with enantiomeric excess up to 99.7%. 展开更多
关键词 optically active 1 1-binaphthalene-2 2-diol L-MENTHOL PHOSPHITE fractional crystal- lization resolution.
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An Efficient Method for α-Alkylation of γ-Butyrolactone
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作者 YuanRuMENG YeDiGUAN 《Chinese Chemical Letters》 SCIE CAS CSCD 2002年第11期1039-1042,共4页
This paper provides a simple, convenient and mild condition method for -alkylation of g-butyrolactone. Three types of (E)-a-alkenyl-g-butyrolactone compounds were synthesized by condensation of corresponding aldehyd... This paper provides a simple, convenient and mild condition method for -alkylation of g-butyrolactone. Three types of (E)-a-alkenyl-g-butyrolactone compounds were synthesized by condensation of corresponding aldehydes and g-butyrolactone, using MeONa and EtONa as base. Then the a-alkyl-g-butyrolactones were gained by reducing the former alkenyl compounds through catalytic transfer hydrogenation under Pd/C catalyst with sodium hypophosphite at room temperature. 展开更多
关键词 Alkylation of -butyrolactone CONDENSATION catalytic transfer hydrogenation Pd / C-sodium hypophosphite.
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Crystal Structure of 3-(4'-Methoxyl)-phenyl-5-cyano-6-methylthio Pyrimidine-2, 4-diones
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作者 刘华银 胡方中 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 北大核心 2001年第3期176-179,共4页
The crystal of the title compound, 3-(4′-Methoxyl)-phenyl-5-cyano-6-methylthio pyrimidine-2, 4-diones, ([C13H11N3O3S]2, Mr=578.62),has been prepared and determined by X-ray diffraction. The crystal belongs to the mo... The crystal of the title compound, 3-(4′-Methoxyl)-phenyl-5-cyano-6-methylthio pyrimidine-2, 4-diones, ([C13H11N3O3S]2, Mr=578.62),has been prepared and determined by X-ray diffraction. The crystal belongs to the monoclinic system, space group P21/n with parameters: a = 11.602(2), b = 15.921(3), c = 13.918(3)?, ( = 94.38(3)(, V = 2563(1) ?3, Z = 4, Dc = 1.499g/cm3, μ(MoK()= 2.64cm-1, F(000)=1200. R and Rw are 0.054 and 0.059, respectively, for 1692 observed unique reflections. The pyrimidione ring is six-membered plane, and the dihedral angle between the pyrimidione ring and benzene ring is 121.05(. From the above result, it could be predicted that the negative atoms among the title compound might interact with target D1 protein, and thus express its inhibitory activity. 展开更多
关键词 pyrimidione crystal structure Hill inhibitory activity
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