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51.
Ivanova А. E. Burgart Ya. V. Saloutin V. I. 《Russian Journal of Organic Chemistry》2018,54(8):1265-1267
Russian Journal of Organic Chemistry - Suzuki cross-coupling was used for modification of 3-polyfluoroalkyl-1-phenylpyrazoles at the position C4. The synthesized 4-bromo- and 4-phenyl derivatives... 相似文献
52.
2,3-Dihydro-1H-1,4-diazepines and 1,2,3,4-tetrahydro-1,4-diazepin-5-ones were obtained by direct condensation of fluorine-containing 1,3-diketones and 1,3-keto ethers, respectively, with ethylenediamine monohydroperchlorate. The structure of the compounds was confirmed by1H NMR, mass spectrometry and molecular weight determination.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 4, pp. 890–896, April, 1991. 相似文献
53.
A safe and simple method for methyl S-arylmercapturate synthesis is described. Thirteen such compounds, to be used afterwards in metabolism studies, have been obtained with yields ranging from 71 to 99.6%. These compounds were obtained using a sulfa-Michael addition and synthesized by adding the corresponding thiophenols to a mixture composed of methyl 2-acetamidoacrylate (MAA), potassium carbonate and a phase transfer catalyst, Aliquat 336. MAA, the initial synthon, was itself isolated in quasi quantitative yield following a fully described synthesis. 相似文献
54.
Russian Chemical Bulletin - Ethyl 2-ethoxymethylidene-3-polyfluoroalkyl-3-oxopropionates under mild conditions undergo regioselective condensation with urea at the ethoxymethylidene substituent... 相似文献
55.
Denis N. Bazhin Yulia S. Kudyakova Yanina V. Burgart Victor I. Saloutin 《Tetrahedron letters》2012,53(15):1961-1963
The unusual transformation of diethyl 2-ethoxymethylenemalonate into triethyl 1,3,5-benzenetricarboxylate is described. This one-pot reaction proceeds in water without any catalyst in a good yield. One of the proposed intermediates of this process is also used under similar conditions to give the desired trisubstituted benzene. A catalyst-free, efficient, practical, and convenient process in water based on deethoxycarbonylation has been developed to form ethyl polyfluorobenzoylacetates in a high yield from diethyl polyfluorobenzoylmalonates. 相似文献
56.
57.
M. V. Pryadeina Ya. V. Burgart V. I. Saloutin P. A. Slepukhin E. V. Sadchikova E. N. Ulomskii 《Russian Journal of Organic Chemistry》2009,45(2):242-247
Methods were developed of the synthesis of alkyl 2-hydroxy-2-fluoroalkyl-4-phenyl-1,2,3,4—tetrahydroimidazo-[1,5-a]pyrimidine-3-carboxylates and alkyl-5-hydroxy-2,7-diphenyl-5-fluoroalkyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine-6-carboxylates by regioselective [3+3]-cycloaddition of 5-aminoimidazole or 5-aminopyrazole to alkyl 2-benzylidene-3-oxo-3-fluoroalkylpropionates at the fluoroacylvinyl fragment. 相似文献
58.
O. G. Khudina Ya. V. Burgart E. V. Shchegol’kov V. I. Saloutin O. N. Kazheva A. N. Chekhlov O. A. D’yachenko 《Russian Journal of Organic Chemistry》2009,45(6):801-809
Steric structure of fluorinated 2-arylhydrazono-3-oxo esters was studied by 1H, 19F, and 13C NMR spectroscopy and X-ray analysis. It was found that these compounds in the crystalline state and in solutions in acetone-d 6, DMSO-d 6, and CDCl3 exist as Z isomers with the ester fragment involved in intramolecular hydrogen bond with the hydrazone NH proton. Exceptions are alkyl 2-arylhydrazono-4,4-difluoro-3-oxobutanoates which exist in acetone-d 6 as mixtures of Z and E isomers, the former prevailing. Unlike fluorinated analogs, ethyl 2-(4-methylphenyl)hydrazono-3-oxobutanoate in crystal has the structure of E isomer in which intramolecular hydrogen bond is formed between the NH proton and acetyl carbonyl group. The same compound in acetone-d 6, DMSO-d 6, and CDCl3 gives rise to a mixture of Z and E isomers, the latter prevailing. 相似文献
59.
Goryaeva M. V. Burgart Ya. V. Saloutin V. I. 《Russian Journal of Organic Chemistry》2010,46(3):432-438
Cyclization of ethyl 2-ethoxymethylidene-3-oxo-3-polyfluoroalkylpropionates with benzimidazol-2-amine in boiling 1,4-dioxane
followed two concurrent pathways with participation of fluoroacyl and ethoxycarbonyl fragments and formation of, respectively,
ethyl 4-hydroxy-4-polyfluoroalkyl-1,4-dihydropyrimido-[1,2-a]benzimidazole-3-carboxylates and 3-polyfluoroacylpyrimido[1,2-a]benzimidazol-4-ols. Dihydropyrimido[1,2-a]benzimidazole derivatives undergo dehydration to give ethyl 4-(polyfluoroalkyl)pyrimido[1,2-a]benzimidazole-3-carboxylates, whereas the hydroxy group in 3-polyfluoroacylpyrimido[1,2-a]benzimidazol-4-ols is capable of being replaced by the amino group of the second benzimidazole molecule with formation of
4-(1H-benzimidazol-2-ylamino)-3-polyfluoroacylpyrimido[1,2-a]benzimidazoles. 相似文献
60.
Ya. V. Burgart A. S. Fokin I. T. Bazyl' V. I. Saloutin 《Russian Chemical Bulletin》1997,46(5):952-954
The reaction of fluoroalkyl-containing 1,3-dicarbonyl compounds with benzylideneacetone with the use of pyridine or triethylamine
as a catalyst gave new 3-fluoroalkyl-4-ethoxycarbonyl(acyl)-5-phenylcyclohexan-3-ol-I-ones in yields of 16–33%.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 5, pp. 992–994, May, 1997. 相似文献