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1.
M. K. Bratenko Yu. V. Kadel’nik V. A. Chornous M. V. Vovk 《Russian Journal of Organic Chemistry》2008,44(2):247-250
Oximes of 4-(4-pyrazolyl)-3-buten-2-onees obtained by successive reaction of 3-aryl-4-formylpyrazoles with acetone and hydroxylamine at the treatment with iodine suffered an oxidative cyclization yielding 3-aryl-4-(5-isoxazolyl)pyrazoles. 相似文献
2.
By reaction of 3-aryl(heteryl)-4-chloromethylpyrazoles with thiourea and sodium thiocyanate respectively 3-aryl(heteryl)-4-mercaptomethylpyrazoles and 3-aryl(heteryl)-thiocyanatomethylpyrazoles were obtained. The latter were subjected to thermal isomerization into 3-aryl(heteryl)-isothiocyanatomethylpyrazoles. 相似文献
3.
3-(3-Aryl-4-formyl-1-pyrazolyl)propionic acids are converted by Knoevenagel condensation under conditions of microwave activation
into 3-[3-aryl-1-(2-ethoxycarbonyl)-4-pyrazolyl]acrylic acids. Reduction of the latter with hydrazine hydrate in the presence
of Raney nickel gives 3-[3-aryl-1-(2-ethoxycarbonyl)-4-pyrazolyl]propionic acids.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 686–690, May, 2006. 相似文献
4.
3-Aryl(heteryl)-4-formylpyrazoles by condensation with malonic acid furnish 3-[3-aryl(heteryl)- pyrazol-4-yl]propenoic acids that in the presence of Raney nickel are reduced by hydrazine hydrate to 3-[3-aryl(heteryl)pyrazol-4-yl]propanoic acids. The successive conversion of both type acids into the corresponding acyl chlorides, esters, and amides was performed. 相似文献
5.
Cyclocondesation of 3-aryl(heteryl)pyrazole-4-carbaldehydes with ethyl acetoacetate and urea (thiourea) in the presence of FeCl3 · 6H2O afforded 3-aryl(heteryl)-4-(4-pyrazolyl)-1,2,3,4-tetrahydropyrimidin-2-ones(thiones).__________Translated from Zhurnal Organicheskoi Khimii, Vol. 41, No. 1, 2005, pp. 97–98.Original Russian Text Copyright © 2005 by Bratenko, Chornous, Vovk. 相似文献
6.
V. A. Chornous A. N. Grozav D. V. Klyukovskii A. V. Bezdudnyi M. V. Vovk 《Russian Journal of Organic Chemistry》2013,49(4):568-574
The reduction of 1-aryl-4-chloro-1H-imidazole-5-carbaldehydes with sodium tetrahydridoborate gave 1-aryl-4-chloro-1H-imidazol-5-ylmethanols which were converted into 5-chloromethyl and 5-fluoromethyl derivatives. 1-Aryl-4-chloro-5-chloromethyl-1H-imidazoles reacted with sodium azide, secondary amines, thiols, and triphenylphosphine to produce the corresponding products of chlorine replacement in the 5-chloromethyl group. 相似文献
7.
V. A. Chornous A. M. Grozav E. B. Rusanov A. M. Nesterenko M. V. Vovk 《Russian Journal of Organic Chemistry》2011,47(5):702-709
1-Alkyl(aryl)imidazolidine-2,4-diones reacted with Vilsmeier-Haack reagent affording 1-alkyl(aryl)-2,4-dichloro-1H-imidazole-5-carbaldehydes whose reactions with sodium azide, sodium alkoholates, with phenols, thiols, and secondary cycloalkylamines
led to the substitution of chlorine in the position 2 of the imidazole ring. The reaction with primary amines resulted in the condensation products at the aldehyde group. 相似文献
8.
Phase composition of the double‐layer Ni‐base and V‐base films obtained and annealed in vacuum of 10‐4–10‐5 Pa within the temperature range of 700–900 K is studied by technique of electronography and transmission electron microscopy. Temperature dependence of resistance and temperature coefficient of resistance (TCR) was investigated. Comparison of TCR experimental data with the calculated data was made at T = 300 K on basis of semiclassical and macroscopic models and formula for TCR of alloys. (© 2004 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim) 相似文献
9.
2-[Alkyl(aryl)amino]acetamides in reaction with Vilsmeier-Haack reagent afforded 1-alkyl(aryl)-4-chloro-1H-imidazole-5-carbaldehydes. 相似文献
10.
V. A. Chornous A. N. Grozav A. V. Bezdudnyi M. V. Vovk 《Russian Journal of Organic Chemistry》2012,48(3):394-398
1-Aryl-4-chloro-1H-imidazole-5-carbaldehydes and 1-aryl-4-chloro-1H-imidazole-5-carboxylic acids reacted with sulfur(IV) fluoride to give, respectively, 1-aryl-4-chloro-5-difluoromethyl- and
1-aryl-4-chloro-5-trifluoromethyl-1H-imidazoles. 相似文献