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3'-Deoxynucleosides. IV. Pyrimidine 3'-deoxynucleosides   总被引:1,自引:0,他引:1  
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A method has been developed for obtaining 3-vinylbenzoxazolinones and 3-vinylbenzoxazolinethione. It has been shown that it is also possible to obtain 3-methylbenzoxazolinethione by this method in good yield (76%).  相似文献   

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A method has been developed for obtaining 3-vinylbenzoxazolinones and 3-vinylbenzoxazolinethione. It has been shown that it is also possible to obtain 3-methylbenzoxazolinethione by this method in good yield (76%).Institute of the Chemistry of Plant Substances, Academy of Sciences of the Uzbek SSR, Tashkent. Translated from Khimiya Prirodnykh Soedinenii, No. 4, pp. 553–556, July–August, 1980.  相似文献   

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The 3-amino-3,5-didesoxy-1,2-O-isopropylidene-α-D -ribofuranose and -β-D -lyxo-furanose and several derivatives thereof have been prepared by hydride reduction of the corresponding oximes.  相似文献   

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Zusammenfassung Mittels der Konversion aromatischer Amine in die entsprechenden Benzaldehyde, einer Methode, die vonBeech entwickelt und von uns auf Haloaniline erweitert wurde, werden in einfacher, eleganter Weise zwei Halogenbenzaldehyde dargestellt.2. Mitt.:S. D. Jolad undS. Rajagopal, Naturwiss.48, 645 (1961).  相似文献   

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Zusammenfassung Zur Untersuchung möglicher Struktur-Wirkungs-Beziehungen in der Reihe der verbrückten Thalidomid-Analoga wurden 36 offenkettige und verkürzte Abkömmlinge der Testsubstanz K 2004 (2) synthetisiert. Die pharmakologische Untersuchung der hergestellten Verbindungen ergab in keinem Falle eine signifikante sedative Aktivität. Dies legt den Schluß nahe, daß die intakte Glutarimid-Struktur bei1 und2 für das Zustandekommen der schlafinduzierenden Wirkung unentbehrlich ist.
Thalidomide analogues
For the evaluation of possible structure-activity relationships in the series of bridged thalidomide analogues 36 openchain and shortended congeners of the test substance K 2004 (2) have been synthesized. The pharmacological evaluation of these compounds revealed in no case any significant sedative activity. This leads to the conclusion that the intact glutarimide structure must be essential for the sleep-inducing activity of1 and2.


Herrn Prof. Dr.M. Pailer zum 60. Geburtstag gewidmet.  相似文献   

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p-Styryldiphenylphosphine was grafted onto polypropylene by γ-radiation. However, olefinic phosphines in general do not readily undergo such grafting. Among the many other olefinic phosphines examined only 1-(4-diphenylphosphinophenyl)-prop-1-ene and vinyldiphenylphosphine were grafted successfully and both had low grafting yields. The optimum conditions for grafting involve low dose rates and high total doses of γ-radiation in dimethylsulfoxide as solvent. This grafting is sensitive to impurities and inhomogeneity in the product readily results, especially at high grafting yields. Oxygen must be rigorously excluded if oxidation of grafted phosphorus(III) to phosphorus (V) is to be avoided. Phosphine oxides can be reduced to phosphines when grafted to the polymer with trichlorosilane. Mass spectrometry has shown that more than one olefinic phosphine binds to a single site in the polymer. Solid-state, high-resolution 31P-NMR is a valuable technique for characterizing the grafted polymer. The preparation and characterization of the following hitherto unreported phosphines is described: In addition, the precursor halides none of which has been reported, were prepared and characterized.  相似文献   

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Referate

Grenzflächenerscheinungen  相似文献   

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