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1.
Data are summarized concerning selective hydrogenation of the pyridine ring in arylpyridines, including those containing silicon, and in annelated pyridines. An effective catalyst, rhenium heptasulfide, has been found, which makes it possible to reduce the pyridine ring without affecting the benzene rings.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 11, pp. 1443–1450, November, 1992. 相似文献
2.
N. S. Prostakov N. M. Mikhailova Yu. M. Talanov 《Chemistry of Heterocyclic Compounds》1970,6(10):1266-1268
The position of the pyridine ring is arylated by reaction of 2,5-dimethyl-4-phenylpyridine with phenyllithium and p-tolyllithium. Destructive oxidation of the diaryl-substituted pyridines primarily affects the pyridine ring.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1359–1361, October, 1970. 相似文献
3.
4.
N. S. Prostakov Keti Sudzhi N. M. Mikhailova L. A. Murugova V. F. Zakharov 《Chemistry of Heterocyclic Compounds》1981,17(10):1038-1042
1-Methyl-1H-indeno[1,2-b]pyridine and 1-methyl-1H-5-(, -dicarbomethoxyvinyl)-(formyl, acetyl)indeno[3,2-b]pyridines were obtained by treatment of N-methyl-4-azafluorenium iodide, as well as mixtures of it with acetylenedicarboxylic ester, dimethylformamide (DMF), and phosphorus oxychloride or acetic anhydride, with bases. 4-Azafluoronenone was used to synthesize 9-(p-methoxyphenyl)-4-azafluoren-9-ol, which was reduced to 9-(p-methoxyphenyl)-4-azafluorene, and 1-methyl-1H-5-(p-methoxyphenyl)indeno[3,2-b]pyridine was obtained from the methiodide of the latter.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1382–1386, October, 1981. 相似文献
5.
N. S. Prostakov B. Kh. Sisimbina S. A. Soldatova V. P. Shalimov K. G. Montenegro N. I. Leonova L. A. Murugova 《Chemistry of Heterocyclic Compounds》1982,18(12):1290-1294
Isomeric (with respect to the position of the nitrogen atom) azafluorenes were cyanoethylated. The resulting 9,9-bis(-cyanoethyl) derivatives were converted to the corresponding dibasic acids and their diesters. The latter were subjected to the Dieckmann reaction to obtain spiro compounds with azafluorene and cyclohexene fragments. The analogous spirans with 1,3-dioxalane and 1,3-dioxane rings were obtained from 3-methyl-2-azafluorenone.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1668–1672, December, 1982. 相似文献
6.
V. V. Kuznetsov A. Pal'ma A. é. Aliev M. Fernandes N. S. Prostakov A. V. Varlamov 《Chemistry of Heterocyclic Compounds》1993,29(6):671-675
The cydization of 1-allyl-1-arylaminocyclohexanes under conditions of acid catalysis afforded 1,2,3,4-tetrahydro-4-methylspiro [quinoline-2-cyclohexanes] methyl (methoxy)-substituted in the phenylene ring. Their mono- and dinitro derivatives were synthesized, and their structure was established. Propositions on the direction of the nitration reaction of these heterocyclic compounds were expressed.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 784–788, June, 1993. 相似文献
7.
N. S. Prostakov A. V. Varlamov M. Torres B. N. Anisimov M. A. Ryashentseva 《Chemistry of Heterocyclic Compounds》1982,18(3):283-284
3-Methyl-4-benzyl-2,6-diphenylpiperidine was obtained by hydrogenation of 3-methyl-4-benzyl-2,6-diphenylpyridine in the presence of rhenium heptasulfide; this confirms the common character of the method of selective hydrogenation of aryl(aralkyl)-substituted pyridine bases to give similarly substituted piperidines. Dehydrocyclization of this pyridine base by heating with sulfur leads to 10-mercapto-1,3-diphenyl-2-azaanthracene, which was obtained under the same conditions from 1,2-diphenyl-1,2-bis(3-methyl-2,6-diphenyl-4-pyridyl)ethane.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 375–376, March, 1982. 相似文献
8.
N. S. Prostakov V. V. Kuznetsov E. E. Stashenko 《Chemistry of Heterocyclic Compounds》1989,25(11):1267-1271
It was established that the yields of a 4-allyl-4-aryl-aminopiperidines in the reaction of 4-aryliminopiperidines with allylmagnesium bromide increase significantly if the reaction is carried out in the presence of a crown ether. A number of previously unknown spiro[tetrahydroquinoline-2,4-piperidines] were obtained in the cyclization of 4-allyl-4-arylaminopiperidines in the presence of sulfuric acid.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 11, pp. 1514–1519, November, 1989. 相似文献
9.
Ammar Mustafa N. M. Mikhailova N. S. Prostakov 《Chemistry of Heterocyclic Compounds》1996,32(1):65-67
9-Phenacylidene-4-azaf luorene and 9-bromo-9-(-bromophenacyl)-4-azafluorene have been used in the synthesis of spiro compounds with fragments of substituted pyrazolines. 1-Methyl-2-oxo-5 phenacylidene-indeno[2, 3-e]-1,2-dihydropyridine and hydrazine gave 1-methyl-2-oxo-3 phenylspiro[indeno(2, 3-e)-1,2-dihydropyridine-5,5-pyrazoline-2]. 相似文献
10.
A. I. Mikaya V. I. Smetanin V. G. Zaikin A. V. Antonova N. S. Prostakov 《Journal of mass spectrometry : JMS》1983,18(3):99-104
A method for structure determination of aliphatic alcohols within mixtures is described. It involves the use of a vapour phase dehydrogenation micro-reactor (Cu, 300°C) located between the chromatographic column and the mass spectrometer or between the injection port and the column. Since primary and secondary alcohols are converted into corresponding carbonyl compounds, they can be readily differentiated from tertiary alcohols and dialkyl ethers. An examination of the mass spectra of alcohols and carbonyl compounds permits the determination of molecular mass, the location of hydroxyl group and the determination of branching at the β-carbon atom. 相似文献