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1.
I. L. Glazko O. P. Gur’yanova S. V. Levanova S. A. Kozlova N. S. Neiman 《Russian Journal of Applied Chemistry》2005,78(6):950-954
A procedure was developed for preparing a plasticizer for polyvinyl chloride compounds from the fraction of dioxane alcohols. The main physicochemical properties of the new plasticizer were determined. Items prepared from formulations containing the new plasticizer were fabricated and tested in laboratory.__________Translated from Zhurnal Prikladnoi Khimii, Vol. 78, No. 6, 2005, pp. 972–976.Original Russian Text Copyright © 2005 by Glazko, Gur’yanova, Levanova, Kozlova, Neiman. 相似文献
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K. A. Volkova A. N. Nikol'skaya E. P. Levanova A. N. Volkov B. A. Trofimov 《Chemistry of Heterocyclic Compounds》1979,15(12):1296-1298
Alkylthio-substituted dienic 1,3-dioxolan-2-ones and bis(4,4-diorganyl-5-methyli-dene-1,3-dioxolan-2-ones) were obtained in high yields by the reaction of 2-methyl-6-alkylthio-5-hexen-3-yn-2-ols and tertiary diacetylenic glycols with carbon dioxide under pressure in the presence of catalytic amounts of triethylamine and monovalent copper salts.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1617–1619, December, 1979.Original article submitted January 24, 1979. 相似文献
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M. G. Voronkov E. P. Levanova E. N. Sukhomazova N. V. Russavskaya E. N. Deryagina N. A. Korchevin 《Russian Journal of Organic Chemistry》2005,41(6):891-893
Gas-phase reaction of bis(2-chloroethyl) sulfide (Yperite) with acetylene at 550–700°C leads to formation of thiophene in 45% yield, the conversion of the initial sulfide being complete. The yield of thiophene reaches 63–68% in the thermolysis of a mixture of acetylene, bis(2-chloroethyl) sulfide, and lower organic disulfides.__________Translated from Zhurnal Organicheskoi Khimii, Vol. 41, No. 6, 2005, pp. 910–912.Original Russian Text Copyright © 2005 by Voronkov, Levanova, Sukhomazova, Russavskaya, Deryagina, Korchevin. 相似文献
4.
E. N. Deryagina E. N. Sukhomazova E. P. Levanova 《Chemistry of Heterocyclic Compounds》2002,38(1):40-45
The effect of methanol and ethanol on the route of the gas-phase reaction of 2-chlorothiophene with hydrogen sulfide, leading to 2-thiophenethiol and to bis(2-thienyl) sulfide, has been investigated. It was found that methanol significantly enhances this reaction and increases its selectivity for the thiol at higher temperatures than without the initiator. The optimal conditions were achieved at 570°C in the presence of 10 mole % of methanol when the conversion of the 2-chlorothiophene in the reaction with hydrogen sulfide reaches 98% and the yield of the thiophenethiol (43%) exceeds that of the bis(2-thienyl)sulfide (31%). In the absence of methanol the 2-thiophenethiol is formed only at 510-540°C in just 17% yield, the basic reaction product being the indicated sulfide (52% yield); the conversion of the 2-chlorothiophene does not exceed 54%. 相似文献
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E. P. Levanova V. A. Grabel’nykh V. S. Vakhrina N. V. Russavskaya A. I. Albanov L. V. Klyba O. A. Tarasova I. B. Rozentsveig N. A. Korchevin 《Russian Journal of General Chemistry》2013,83(9):1660-1665
Dimethyldiselenide reacts with 2,3-dichloro-1-propene at 20–25°C in the hydrazine hydrate-KOH medium to form 2-chloro-3-methylselanyl-1-propene with 90% yield. Diphenyldiselenide in the reaction with 2,3-dichloro-1-propene, depending on the conditions, can give quite selectively four products: 2-chloro-3-phenylselanyl-1-propene, phenylselanylpropadiene, 1-phenylselanyl-1-propyne, and Z-1,2-bis(phenylselanyl)-1-propene. The effect of the selenium atom on the reaction direction and the products structure is discussed. 相似文献
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E. P. Levanova V. A. Grabel’nykh V. S. Vakhrina N. V. Russavskaya A. I. Albanov I. B. Rozentsveig N. A. Korchevin 《Russian Journal of General Chemistry》2014,84(3):439-443
Dibenzyldisulfide and -diselenide react with 2,3-dichloro-1-propene in the system hydrazine hydrate-KOH by the domino mechanism: nucleophilic substitution of the allyl chlorine, dehydrochlorination with participation of the chlorine atom at the sp 2-carbon atom, allene-acetylene rearrangement, nucleophilic addition of the chalcogenide reagent to the triple bond. The effect of the nature of the chalcogen atom and the benzyl substituent on the studied domino reaction is discussed. 相似文献
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E. P. Levanova V. A. Grabel’nykh A. V. Elaev N. V. Russavskaya L. V. Klyba A. I. Albanov N. A. Korchevin 《Chemistry of Heterocyclic Compounds》2012,47(11):1345-1352
The saturated heterocyclic compounds C4H8Y, C5H10Y, and C5H10Y2 (Y = Se or Te) have been prepared by the reaction of 1,4-dibromobutane or 1,5-dibromopentane with potassium chalcogenides.
The novelty of the route consists of the use of the hydrazine hydrate–KOH system for the reductive generation of potassium
selenide, telluride, diselenide or ditelluride from elemental chalcogens. 相似文献