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1.
Инвентарный номер: нет.
   
   H 62


   
    Heterocyclization of Fluorinated Di- and Tricarbonyl Compounds [Text] : доклад, тезисы доклада / Ya. V. Burgart, O. G. Kuzueva, A. S. Fokin, V. I. Saloutin // International Memorial I.Postovsky Conference on Organic Chemisty, Ekaterinburg, March 17-20, 1998 : program and abstracts. - Ekaterinburg, 1998. - P51
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ

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2.
Инвентарный номер: нет.
   
   S 98


   
    Synthesis of fluorinated 2(3)-arylhydrazones of 1,2,3-tri(1,2,3,4-tetra)carbonyl compounds and their heterocyclization reactions [] / Ya. V. Burgart, A. S. Fokin, O. G. Kuzueva, O. N. Chupakhin, V. I. Saloutin // Journal of Fluorine Chemistry. - 1998. - Vol. 92, № 2. - С. 101-108
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: New fluorinated 2-arylhydrazones of 1,2,3-triketones, 2-arylhydrazone-1,2,3-diketo esters and 3-arylhydrazone-1,2,3,4-triketo esters have been prepared by the coupling of fluorine-containing 1,3-keto esters, 1,3-diketones, acyl(aroyl)pyruvic esters and their chelates with aryldiazonium chlorides. The arylhydrazones react with hydrazine hydrate, phenylhydrazine, thiosemicarbazide and hydroxylamine to form the corresponding pyrazole and isoxazole derivatives. Interaction of 3-arylhydrazone-1,2,3,4-diketo esters with o-phenylenediamine results in quinoxaline products. Intramolecular cyclization of the arylhydrazones with pentafluorophenyl substituents leads to cinnolone derivatives

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3.
Инвентарный номер: нет.
   
   P 43


   
    Perfluoroepoxyoxolanes in the synthesis of fluorine-containing heterocycles [Electronic resource] / V. I. Filyakova, A. Ya. Zapevalov, M. I. Kodess, P. A. Slepukhin, V. I. Saloutin // Russian Journal of Organic Chemistry (Translation of Zhurnal Organicheskoi Khimii). - 2009. - Vol. 45, № 6. - P884-889. - Bibliogr. : p. 889 (15 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
PERFLUOROEPOXYOXOLANES -- HETEROCYCLES -- FLUORINE-CONTAINING HETEROCYCLES -- NUCLEOPHILES -- DIFUNCTIONAL NUCLEOPHILES -- OXIRANE RING
Аннотация: Perfluoro-3,4-epoxyoxolane and 3,4-epoxy-2- trifluoromethylpentafluorooxolane readily reacted with difunctional nucleophiles via opening of the oxirane ring and subsequent heterocyclization. Their reactions with thiourea and o-phenylenediamine gave new fluorine-containing fused heterocyclic compounds 2-amino-3a-hydroxy-4,4,6,6,6a-pentafluoro-3a,4,6, 6a-tetrahydrofuro[3,4-d][1,3]thiazole and 1,1,3,3-tetrafluoro- and 1-trifluoromethyl-1,3,3-trifluoro-1,3-dihydrofuro[3,4-b]quinoxalines, respectively. The molecular and crystalline structures of the products were determined by X-ray analysis.

\\\\Expert2\\nbo\\Russian Journal of Organic Chemistry\\2009, 45 (6), 884.pdf
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4.
Инвентарный номер: нет.
   
   R 30


   
    Reaction of 3-(polyfluoroacyl)chromones with hydrazines: new regioselective synthesis of RF-containing pyrazoles [Electronic resource] / V. Ya. Sosnovskikh, R. A. Irgashev, V. S. Moshkin, M. I. Kodess // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2008. - Vol. 57, № 10. - P2146-2155
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Reactions of 3-(polyfluoroacyl)chromones with hydrazine, methyl-and phenylhydrazines proceed by the mechanism of nucleophilic 1,4-addition with subsequent pyrone ring opening and heterocyclization at the polyfluoroacyl group to 4-(2-hydroxyaroyl)-3-polyfluoro-alkylpyrazoles or at the aroyl group to 4-polyfluoroalkyl-2,4-dihydrochromeno[4,3-c]pyrazol-4-ols. Regiochemistry of the products was established based on the data of 2D-experiments HSQC, HMBC, and NOESY and X-ray diffraction study

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2008, 57 (10), 2146.pdf
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5.
Инвентарный номер: нет.
   
   K 45


    Kim, D. G.
    Tandem heterocyclization in the synthesis of novel imidazo[1,5-d][1,3,4]thiadiazine / D. G. Kim, E. S. Ilinykh, P. A. Slepukhin // Chemistry of Heterocyclic Compounds. - 2011. - Vol. 46, № 11. - P1418-1419
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
1,3,4-THIADIAZOLE -- 7-AMINO -- THIADIAZINIUM PENTAIODIDE

\\\\Expert2\\nbo\\Chemistry of Heterocyclic Compounds\\2011, v.46, N 11, p.1418-1419.pdf
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6.
Инвентарный номер: нет.
   
   F 94


    Frolova, T. V.
    Heterocyclization of 5-ethyl- 2-methallylthio-6-methyl-4(3H)-pyrimidinone using acids / T. V. Frolova, P. A. Slepukhin, D. G. Kim // Chemistry of Heterocyclic Compounds. - 2011. - Vol. 47, № 2. - P252-254. - Bibliogr. : p. 253-254 (6 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
X-RAY STRUCTURAL ANALYSIS ???? -- 4(3H)-PYRIMIDINONES -- HETERO-CYCLIZATION

\\\\Expert2\\nbo\\Chemistry of Heterocyclic Compounds\\2011, v.47, N 2, p.252-254.pdf
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7.
Инвентарный номер: нет.
   
   S 98


   
    Synthesis of fluorine-containing allantoins, hydantoins, and oxazolones from terminal perfluoroolefin oxides and urea / L. V. Saloutina, A. Ya. Zapevalov, M. I. Kodess, V. I. Saloutin, O. N. Chupakhin // Russian Journal of Organic Chemistry (Translation of Zhurnal Organicheskoi Khimii). - 2012. - Vol.48, №3. - С. 387-393
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
ALLANTOINS -- HYDANTOINS -- OXAZOLONES
Аннотация: 1,2-Epoxyoctafluorobutane reacted with urea in DMSO and aqueous DMSO, dioxane, and acetonitrile to give 40–42% of 5-hydroxy-5-pentafluoroethylimidazolidine-2,4-dione. 5-Hydroxy-5-tridecafluorohexylimidazolidine-2,4-dione was formed in 54% yield in analogous reaction of 1,2-epoxytridecafluorooctane with urea in aqueous DMSO. The reactions of 1,2-epoxyoctafluorobutane and 1,2-epoxytridecafluorooctane with urea in anhydrous dioxane and acetonitrile unexpectedly afforded heterocyclization products, 2-amino-5-fluoro-5-perfluoroalkyloxazol-4(5H)-ones (yield 11–82%). Fluorine-containing allantoin, 5-tridecafluorohexyl-5-ureidoimidazolidine-2,4-dione (yield 19%), and N-(1-hydroxy-2,2,3,3,4,4,5,5,6,6,7,7,7-tridecafluoroheptyl)-urea (yield 46%) were synthesized for the first time by reaction of 1,2-epoxytridecafluoroctane with urea in DMSO and aqueous DMSO

\\\\Expert2\\nbo\\Russian Journal of Organic Chemistry\\2012, 48 (3), 387-393.pdf
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8.
Инвентарный номер: нет.
   
   U 62


   
    Unusual heterocyclization of chalcone podands with 3-amino-1,2,4-triazole / I. G. Ovchinnikova, M. S. Valova, E. G. Matochkina, M. I. Kodess, A. A. Tumashov, P. A. Slepukhin, O. V. Fedorova, G. L. Rusinov, V. N. Charushin // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2011. - Vol.60, №5. - С. 965-974
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
TEMPLATE SYNTHESIS -- CHALCONE PODAND -- CROWN ETHERS
Аннотация: A new type of intramolecular cyclization of 1,5-bis[2-(E-3-oxo-3-phenylprop-1-enyl)-phenoxy]-3-oxapentane with 3-aminotriazole promoted by potassium ions was discovered. A cascade mechanism for the formation of crownophane with 4,7-dihydro[1,2,4]triazolo[1,5-a]-pyrimidine fragment was suggested. Effects of oligooxyethylene fragment of the chalcone podand and acid-base catalysis on the selectivity of the cyclocondensation processes and degree of oxidation of triazolopyrimidine fragments were studied. The product structures were confirmed by IR, 1H and 13C NMR spectroscopy and X-ray diffraction study

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2011, 60 (5), 965-974.pdf
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9.
Инвентарный номер: нет.
   
   F 62


   
    Five-membered 2,3-dioxoheterocycles: LXXXVI. Spiro-heterocyclization of 1-aryl-4-aroyl-5-methoxycarbonyl-1H-pyrrole-2,3-diones under the action of 3-arylamino-1H-inden-1-ones. Crystal and molecular structure of 4′-hydroxy-3′-(2,4-dimethylbenzoyl)-1,1′-diphenyl-1H-spiro[indeno[1,2-b]pyrrole-3,2′-pyrrole]-2,4,5′(1′H)-trione / N. V. bubnov, E. S. Denislamova, P. A. Slepukhin, A. N. Maslivets // Russian Journal of Organic Chemistry (Translation of Zhurnal Organicheskoi Khimii). - 2012. - Vol.48, №5. - С. 694-698
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
SPIRO-HETEROCYCLIZATION -- METHOXYCARBONYL -- INDOLE
Аннотация: 1-Aryl-4-aroyl-5-methoxycarbonyl-1H-pyrrole-2,3-diones react with 3-arylamino-1H-inden-1-ones affording 1,1′-diaryl-3′-aroyl-4′-hydroxy-1H-spiro[indeno[1,2-b]pyrrole-3,2′-pyrrole]-2,4,5′(1′H)-triones. The crystal and molecular structure of 4′-hydroxy-3′-(2,4-dimethylbenzoyl)-1,1′-diphenyl-1H-spiro[indeno[1,2-b] pyrrole-3,2′-pyrrole]-2,4,5′(1′H)-trione

\\\\Expert2\\nbo\\Russian Journal of Organic Chemistry\\2012, 48 (5), 694-698.pdf
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10.
Инвентарный номер: нет.
   
   F 62


   
    Five-membered 2,3-dioxo heterocycles: XCIII. Spiro heterocyclization of 4,5-diaroyl-1H-pyrrole-2,3-diones with acyclic enamine. Crystalline and molecular structure of substituted 1,7-diazaspiro[4.4]nonane [Electronic resource] / P. S. Silaichev, N. V. Kudrevatykh, P. A. Slepukhin, A. N. Maslivets // Russian Journal of Organic Chemistry (Translation of Zhurnal Organicheskoi Khimii). - 2013. - Vol.49, №6. - С. 860-863. - Bibliogr. : p. 863 (7 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
2,3-DIOXOHETEROCYCLES -- SPIRO-HETEROCYCLIZATION -- 2,3-DIONES
Аннотация: 4,5-Diaroyl-1-aryl-1H-pyrrole-2,3-diones reacted with ethyl 3-amino-3-phenylprop-2-enoate to give ethyl 4-aroyl-1,6-diaryl-3-hydroxy-2-oxo-8-phenyl-1,7-diazaspiro[4.4]nona-3,6,8-triene-9-carboxylates. The crystalline and molecular structures of ethyl 4-benzoyl-3-hydroxy-1-(4-methylphenyl)-2-oxo-6,8-diphenyl-1,7-diazaspiro[4.4]nona-3,6,8-triene-9-carboxylate were determined by X-ray analysis

\\\\expert2\\NBO\\Russian Journal of Organic Chemistry\\2013, 49, (6), 860-863.pdf
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