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1.
Инвентарный номер: нет.
   
   A 62


   
    Antifriction properties of new fluorine-containing derivatives of natural graphite / T. I. Gorbunova, A. Ya. Zapevalov, D. N. Bazhin, L. G. Korshunov, V. S. Gaviko, V. I. Saloutin // Russian Journal of Applied Chemistry. - 2012. - Vol.85, №1. - С. 102-107
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
ANTIFRICTION PROPERTIES -- FLUORINE-CONTAINING DERIVATIVES -- GRAPHITE
Аннотация: Interaction of natural graphite with potassium salts of perfl uoro(ω-chloroperfl uoro)carboxylic acids in the presence of potassium persulfate was studied. The derivatives obtained were used as independent lubricants for a chromium-containing-steel friction pair

\\\\Expert2\\nbo\\Russian Journal of Applied Chemistry\\2012, v. 85, N 1, p.102.pdf
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2.
Инвентарный номер: нет.
   
   R 30


   
    Reaction of methyl 1-bromocyclohexanecarboxylate with zinc and 3-aryl-2-cyanopropenoic acids amides / N. F. Kirillov, M. E. Nikiforova, S. N. Shurov, P. A. Slepukhin, M. I. Vakhrin // Russian Journal of General Chemistry. - 2012. - Vol.82, №7. - С. 1228-1232
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
BROMOCYCLOHEXANECARBOXYLATE -- ZINC -- CYANOPROPENOIC ACIDS
Аннотация: Methyl 1-bromocyclohexanecarboxylate reacts with zinc and amides or methylamides of 3-aryl-2-cyanopropenoic acids to give 5-aryl-1,3-dioxo-2-azaspiro[5.5]undecane-4-carbonitriles or 5-aryl-2-methyl-1,3-dioxo-2-azaspiro[5.5]undecane-4-carbonitriles

\\\\Expert2\\nbo\\Russian Journal of General Chemistry\\2012, V. 82, N 7, p. 1228–1232.pdf
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3.
Инвентарный номер: нет.
   
   S 98


   
    Synthesis and the molecular and crystal structures of methyl 2-substituted 7,7-dimethyl-5-oxo-5,6,7,8-tetrahydroquinoline-4-carboxylates [Electronic resource] / D. A. Rudenko, M. V. Artemova, P. A. Slepukhin, V. I. Karmanov, S. N. Shurov // Chemistry of Heterocyclic Compounds. - 2013. - Vol.48, №9. - P1321-1324
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
SYNTHESIS -- MOLECULAR STRUCTURE -- CRYSTAL STRUCTURE
Аннотация: Methyl 7,7-dimethyl-5-oxo-5,6,7,8-tetrahydroquinoline-4-carboxylates were obtained as a result of 3-amino-5,5-dimethylcyclohex-2-enone reaction with the methyl esters of acyl(aroyl)pyruvic acids. The structure of methyl 7,7-dimethyl-5-oxo-2-phenyl-5,6,7,8-tetrahydroquinoline-4-carboxylate was established by X-ray structural analysis

\\\\Expert2\\NBO\\Chemistry of Heterocyclic Compounds\\2013, v.48, N 9, p. 1321-1324.pdf
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4.
Инвентарный номер: нет.
   
   S 98


   
    Synthesis of 5-substituted 8,8-dimethyl-8,9-dihydro-3H,7H-[1,2]oxazino[5,4,3-de]quinolin-3-ones [Electronic resource] / D. A. Rudenko, P. A. Slepukhin, V. I. Karmanov, M. I. Vakhrin, S. N. Shurov, Yu. A. Shchurov // Chemistry of Heterocyclic Compounds. - 2013. - Vol.48, №10. - 1539-1544.
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
HYDROXYLAMINE -- QUANTUM-CHEMICAL CALCULATIONS -- TETRAHYDROQUINOLINE-4-CARBOXYLIC ACIDS
Аннотация: The reaction of 2-substituted 7,7-dimethyl-5-oxo-5,6,7,8-tetrahydroquinoline-4-carboxylic acids with hydroxylamine results in the formation of 5-substituted 8,8-dimethyl-8,9-dihydro-3H,7H-[1,2]ox-azino[5,4,3-de]quinolin-3-ones. The structure of the 5-phenyl derivative has been established by X-ray structural analysis. A possible mechanism of the reaction has been proposed on the basis of nonempirical quantum-chemical calculations

\\\\Expert2\\NBO\\Chemistry of Heterocyclic Compounds\\2013, v.48, N 10, p. 1539-1544.pdf
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5.
Инвентарный номер: нет.
   
   S 98


   
    Synthesis of enantiomers of 6-nitro- and 6-amino-2-methyl-1,2,3,4-tetrahydroquinolines / D. A. Gruzdev, G. L. Levit, M. I. Kodess, V. P. Krasnov // Chemistry of Heterocyclic Compounds. - 2012. - Vol.48, №5. - С. 748-757
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
AMIDES -- DIASTEREOISOMERS -- ENANTIOMERS
Аннотация: Enantiomers of 2-methyl-6-nitro-1,2,3,4-tetrahydroquinoline have been obtained by kinetic resolution of racemic 2-methyl-1,2,3,4-tetrahydroquinoline in acylation with acyl chlorides of N-protected amino acids followed by regioselective nitration of the diastereoisomeric amides and acidic hydrolysis. The introduction of a trifluoroacetyl protecting group into the position 1 of the enantio pure nitro compound followed by the reduction led to (S)-6-amino-2-methyl-1-trifluoroacetyl-1,2,3,4-tetra-hydroquinoline in a high yield

\\\\Expert2\\nbo\\Chemistry of Heterocyclic Compounds\\2012, v.48, N 5, p.748-757.pdf
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6.
Инвентарный номер: нет.
   
   C 21


   
    Carboxyalkylation of chitosan in the gel state / Yu. A. Skorik, A. V. Pestov, M. I. Kodess, Yu. G. Yatluk // Carbohydrate Polymers. - 2012. - Vol. 90, № 2. - С. 1176-1181
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
CHITOSAN -- CHEMICAL MODIFICATION -- GEL TECHNIQUE
Аннотация: This study presents a new approach for direct carboxyalkylation of chitosan in the gel state by using aza-Michael addition and substitution reactions. Various reagents were applied including acrylic and crotonic acids, and alpha-, beta-, gamma-, delta-, and epsilon-halocarboxylic acids. The reaction of chitosan with gamma- and delta-halocarboxylic acids showed no target product formation either in solution or in the gel state. In the case of acrylic, crotonic, alpha- and beta-halocarboxylic acids, the reaction performed in the gel state (concentration of chitosan 20-40%) shows higher degree of substitution at lower reaction time and temperature than in diluted solutions (concentration of chitosan 0.5-2%). The results were discussed in terms of kinetics of the target and side reactions. H-1 and C-13 NMR confirmed that in all cases the carboxyalkylation of chitosan proceeds exclusively at the amino groups

\\\\Expert2\\nbo\\Carbohydrate Polymers\\2012, v. 90, p.1176.pdf
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7.
Инвентарный номер: нет.
   


   
    1,3-Dipolar cycloadditions of nonstabilised azomethine ylides at 3-substituted coumarins: synthesis of 1-benzopyrano[3,4-c]pyrrolidines / V. S. Moshkin, V. Ya. Sosnovskikh, P. A. Slepukhin, Gerd-Volker Röschenthalerc // Mendeleev Communications. - 2012. - Vol.22, №1. - С. 29-31
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
COUMARINS -- AZOMETHINE YLIDES -- PYRROLIDINES
Аннотация: Reaction of 3-substituted coumarins with N-alkyl-α-amino acids and aldehydes proceeds regio- and stereoselectively to give 1-benzopyrano[3,4-c]pyrrolidines as a result of 1,3-dipolar cycloaddition of the intermediate azomethine ylides at the Δ3-bond of the coumarins

\\\\Expert2\\nbo\\Mendeleev Communications\\2012, v.22, p. 29.pdf
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8.
Инвентарный номер: нет.
   
   S 98


   
    Synthesis of 2-substituted 7,7-dimethyl-5-oxo-5,6,7,8-tetrahydroquinoline-4-carboxylic acids / D. A. Rudenko, S. N. Shurov, M. I. Kodess, M. A. Ezhikova, A. N. Vasyanin // Russian Journal of Organic Chemistry (Translation of Zhurnal Organicheskoi Khimii). - 2012. - Vol.48, №6. - С. 799-803
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
SYNTHESIS -- TETRAHYDROQUINOLINE -- CARBOXYLIC ACIDS
Аннотация: 2-Substituted 7,7-dimethyl-5-oxo-5,6,7,8-tetrahydroquinoline-4-carboxylic acids were synthesized by reaction of acyl- and aroylpyruvic acids with 3-amino-5,5-dimethylcyclohex-2-en-1-one. A plausible mechanism of their formation was proposed on the basis of ab initio quantum-chemical calculations

\\\\Expert2\\nbo\\Russian Journal of Organic Chemistry\\2012, 48 (6), 799-803.pdf
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9.
Инвентарный номер: нет.
   
   P 49


    Pestov, A. V.
    Comparative coordination ability of N-(2-hydroxyethyl)aminoacetic acid and O-(2-hydroxyethyl)hydroxyacetic acid in the copper(II) complexes [Electronic resource] / A. V. Pestov, P. A. Slepukhin, Yu. G. Yatluk // Russian Journal of Coordination Chemistry. - 2012. - Vol.38, №12. - P738-743
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
COPPER(II) -- N-(2-HYDROXYETHYL)AMINOACETIC -- O-(2-HYDROXYETHYL)HYDROXYACETIC ACIDS
Аннотация: Copper(II) complexes based on N-(2-hydroxyethyl)aminoacetic and O-(2-hydroxyethyl)hydroxyacetic acids were synthesized. Their structures were studied by X-ray diffraction analysis. The coordination spheres of the copper metal center were compared in the condensed phase for the both ligands

\\\\Expert2\\NBO\\Russian Journal of Coordination Chemistry\\2012, v. 38, N. 12, p.738.pdf
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10.
Инвентарный номер: нет.
   
   N 89


   
    Novel synthetic routes to N-(2-amino-9H-purin-6-yl)-substituted amino acids [Electronic resource] / A. Yu. Vigorov, V. P. Krasnov, D. A. Gruzdev, A. A. Men'shikova, A. M. Demin, G. L. Levit, V. N. Charushin // Mendeleev Communications. - 2014. - Vol.24, №1. - С. 35-36. - Bibliogr. : p. 36 (22 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
2-AMINOPURINES -- 2-AMINO-6-CHLOROPURINE -- AMINO ACIDS
Аннотация: Reaction of N2-protected 2-amino-6-chloropurine with tert-butyl (S)-phenylalaninate, (R)- and (S)-valinates followed by deprotection affords 2-aminopurines bearing at 6-position the corresponding amino acid moieties, whose chiral centre is partially racemized

\\\\expert2\\nbo\\Mendeleev Communications\\2014, v.24, p. 35.pdf
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11.
Инвентарный номер: нет.
   
   A 19


   
    Acylative kinetic resolution of racemic amines with profens and amino acids derivatives / V. P. Krasnov, G. L. Levit, D. N. Kozhevnikov, M. I. Kodess, D. A. Gruzdev, E. N. Chulakov, V. N. Charushin // International Congress on Organic Chemistry, dedicated to the 150-th anniversary of the Butlerov's Theory of Chemical Structure of Organic Compounds, Kazan, September 18-23, 2001 : book of abstr. - Kazan, 2011. - С. 85
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
KINETIC RESOLUTION -- S-AMINES -- RACEMIC AMINES

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12.
Инвентарный номер: нет.
   
   S 98


   
    Synthesis, photophysical and electrochemical properties of novel 6,12-di(thiophen-2-yl) substituted indolo[3,2-b]carbazoles [Electronic resource] / R. A. Irgashev, A. Yu. Teslenko, E. F. Zhilina, A. V. Schepochkin, O. S. Eltsov, G. L. Rusinov, V. N. Charushin // Tetrahedron. - 2014. - Vol.70, №31. - С. 4685-4696
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
INDOLO[3,2-B]CARBAZOLE -- INDOLE -- THIOPHENE
Аннотация: Novel 5,11-dialkyl-6,12-di(thiophen-2-yl) substituted 5,11-dihydroindolo[3,2-b]carbazoles have been obtained and plausible ways for their further modifications via the Friedel–Crafts reaction are presented. The formylation of these indolo[3,2-b]carbazoles with dichloromethyl alkyl esters catalysed by Lewis acids leads to the formation of the corresponding 2,8-diformyl derivatives. Applicability of this formylation method for modification of indolo[3,2-b]carbazoles bearing electron-rich aromatic substituents at C-6 and C-12 has also been demonstrated. The Knoevenagel condensation of 2,8-dialdehydes with active methylene nitriles has been studied. The measurements of optical and redox properties for a number of new indolo[3,2-b]carbazoles have been performed

\\\\expert2\\nbo\\Tetrahedron\\2014, v. 70 , p. 4685-4696.pdf
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13.
Инвентарный номер: нет.
   
   E 31


    Egorov, I. N.
    Synthesis of chiral pyrimidin-2(1H)-Ones from n-Carbamoyl amino acids [Electronic resource] / I. N. Egorov, V. L. Rusinov, O. N. Chupakhin // Zeitschrift fur Naturforschung - Section B. Journal of Chemical Science. - 2013. - Vol.68, №11. - С. 1253-1258. - Bibliogr. : p. 1258 (15 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
AMINO ACIDS -- CHIRALITY -- CONDENSATION
Аннотация: A series of previously unknown pyrimidin-2(1H)-ones containing chiral amino acid fragments was synthesized from 1,1,3,3-tetramethoxypropane and N-carbamoyl derivatives of amino acids under acidic conditions

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14.
Инвентарный номер: нет.
   
   D 38


    Demin, A. M.
    Covalent surface modification of Fe3O4 magnetic nanoparticles with alkoxy silanes and amino acids [Электронный ресурс] / A. M. Demin, V. P. Krasnov, V. N. Charushin // Mendeleev Communications. - 2013. - Vol.23, №1. - P14-16
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
Fe3O4 -- MAGNETIC NANOPARTICLES -- ALKOXY SILANES
Аннотация: (3-Aminopropyl)silane-modified magnetic nanoparticles containing ε-aminocaproic acid and l-lysine fragments with free functional groups were obtained by the surface modification of Fe3O4 with alkoxysilane derivatives

\\\\Expert2\\NBO\\Mendeleev Communications\\2013, v.23, p. 14.pdf
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15.
Инвентарный номер: нет.
   
   S 98


   
    Synthesis of photochromic 6-aryl-substituted bis(benzothiophenyl)- perfluorocyclopentenes by the Suzuki-Miyaura cross-coupling [Электронный ресурс] / M. M. Krayushkin, A. M. Bogacheva, K. S. Levchenko, O. I. Kobeleva, T. M. Valova, V. A. Barachevskii, J. L. Pozzo, V. N. Charushin // Mendeleev Communications. - 2013. - Vol.23, №2. - P78-80
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
SYNTHESIS -- PHOTOCHROMIC -- CROSS-COUPLING
Аннотация: The Suzuki cross-coupling of 1,2-bis(6-iodo-2-methylbenzo[b]thiophen-3-yl) hexafluorocyclopentene and (het)arylboronic acids depending on the reaction conditions affords bis- or mono-adducts. The latter on next cross-coupling with different boronic acid give unsymmetrical dihetarylethenes. Spectral-kinetic studies of the photoinduced cyclization of the compounds obtained were performed

\\\\Expert2\\NBO\\Mendeleev Communications\\2013, v.23, p. 78.pdf
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16.
Инвентарный номер: нет.
   
   H 65


   
    Highly diastereoselective 1,3-dipolar cycloaddition of nonstabilized azomethine ylides to 3-nitro-2-trihalomethyl-2H-chromenes: synthesis of 1-benzopyrano[3,4-c]pyrrolidines [Electronic resource] / V. Yu. Korotaev, A. Yu. Barkov, V. S. Moshkin, E. G. Matochkina, M. I. Kodess, V. Ya. Sosnovskikh // Tetrahedron. - 2013. - Vol.69, №40. - P8602-8608. - Bibliogr. : p. 8608 (13 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
3-NITRO-2H-CHROMENES -- NONSTABILIZED AZOMETHINE YLIDES -- 1,3-DIPOLAR CYCLOADDITION
Аннотация: Reactions of 3-nitro-2-trifluoro(trichloro)methyl-2H-chromenes, including 2-unsubstituted derivatives, with N-alkyl-α-amino acids (sarcosine, proline) and paraformaldehyde proceed diastereoselectively to give 1-benzopyrano[3,4-c]pyrrolidines in good yields as a result of a 1,3-dipolar cycloaddition of the intermediate nonstabilized azomethine ylide at the Δ3-bond of the chromene system

\\\\expert2\\NBO\\Tetrahedron\\2013, v. 69, p. 8602.pdf
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17.
Инвентарный номер: нет.
   
   C 21


   
    Carboxyethenylation of polychlorobiphenyls / A. Mechaev, A. V. Pestov, Yu. G. Yatluk, M. G. Pervova, A. A. Panyukova // Russian Journal of Organic Chemistry (Translation of Zhurnal Organicheskoi Khimii). - 2013. - Vol.49, №5. - С. 691-695. - Библиогр.: с. 695 (12 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
BUTYL ACRYLATE -- PALLADIUM CATALYSTS -- POLYCHLOROBIPHENYLS
Аннотация: For the first time 2-carboxyethenylation was performed with butyl acrylate in the presence of palladium catalysts of bromine derivatives of polychlorobiphenyls obtained by bromination of polychlorobiphenyls. The haloderivatives of the butyl phenylcinnamate are readily hydrolyzed and hydrodehalogenized affording a mixture of phenylhydrocinnamic acids

\\\\expert2\\NBO\\Russian Journal of Organic Chemistry\\2013, 49, (5), 691-695.pdf
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18.
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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19.
Инвентарный номер: нет.
   
   O-84


    Osintseva, E. V.
    Protolytic properties and complexation with copper(II) ions of some azo derivatives of beta-arylaminopropionic acids [Electronic resource] / E. V. Osintseva, L. K. Neudachina, Yu. G. Yatluk // Russian Journal of Inorganic Chemistry (Zhurnal Neorganicheskoi Khimii). - 2010. - Vol. 55, № 10. - P1644-1650
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The azo coupling reaction of N-(2-carboxyethyl)anthranilic acid and N,N,N,N-tetrabis(2-carboxyethyl)-1,3-phenylenediamine with diazosulfanilic acid yielded the complexones sodium 4-N-(2-carboxyethyl)amino-5-carboxyazobenzene-4?-sulfonate (I) and 2,4-N,N,N,N-tetrabis(2-carboxyethyl)diaminoazobenzene-4?-sulfonic acid (II), respectively. The acidity constants of I and II (20°C = 0.1M KCl) were determined to be as follows: for I, pK 00 = 1.29 ± 0.13, pK 0 = 2.92 ± 0.07, pK 1 = 3.92 ± 0.05, pK 2 = 5.16 ± 0.03; for II, pK 00 = 2.35 ± 0.06, pK 0 = 2.81 ± 0.09, pK 1 = 3.21 ± 0.11, pK 2 = 3.81 ± 0.09, pK 3 = 4.34 ± 0.04, pK 4 = 5.03 ± 0.06, pK 5 = 6.67 ± 0.07. The electronic absorption spectra of I and II were measured, and acid-base equilibrium scheme for I and II in aqueous solutions were suggested. The complexation constants of I and II with copper(II) ions were determined to be logK CuQI= 5.47 ± 0.06 and logK CuQII= 5.72 ± 0.13 (20°C = 0.1 M KCl). ??

\\\\Expert2\\nbo\\Russian Journal of Inorganic Chemistry\\2010, v. 55, N 10, с.1644.pdf
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20.
Инвентарный номер: нет.
   
   A 18


   
    Acid-base properties and prototropic tautomerism of isomeric 1,2,4-triazin-3- and -5-ones [Electronic resource] / I. V. Khabibulina, R. E. Trifonov, A.P. Volovodenko, M. S. Eremenkova, O. N. Chupakhin, V. L. Rusinov, G. V. Zyryanov, V. A. Ostrovskii // Russian Journal of Organic Chemistry (Translation of Zhurnal Organicheskoi Khimii). - 2004. - Vol. 40, № 3. - P426-430. - Bibliogr. : p. 430 (40 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
ACID -- BASE -- TRIAZINE DERIVATIVE -- AQUEOUS SOLUTION
Аннотация: The acidity and basicity constants of isomeric phenyl(aryl)-1,2,4-triazin- 3- and -5-ones in aqueous solution were determined by spectrophotometry: pK a = 7.3-6.2; pKBH+ = 0.1 to -2.2. 1,2,4-Triazin-3-ones are weaker bases than the corresponding 1,2,4-triazin-5-ones. According to the AM1 calculations, the most thermodynamically favorable tautomer in the gas phase is the oxo form: namely, 2H-tautomers of the neutral bases and 2,4-H,H +-tautomers of the conjugate acids.

\\\\Expert2\\nbo\\Russian Journal of Organic Chemistry\\2004, 40 (3), 426.pdf
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Сиглы отделов ЦНБ УрО РАН


  бр.ф. - Бронированный фонд

  бф - Научно-библиографический отдел

  БХЛ - Фонд художественной литературы

  ИИиА -Фонд исторической литературы в ЦНБ УрО РАН

  ИМЕТ -Отдел ЦНБ в Институте металлургии УрО РАН

  кх - Отдел фондов (книгохранениe)

  МБА - Межбиблиотечный абонемент

  мф - Методический фонд

  ок - Отдел научной каталогизации

  оку - Отдел комплектования и учета

  орф - Обменно-резервный фонд

  пф - Читальный зал деловой и патентной информации

  рк - Фонд редкой книги

  ч/з - Главный читальный зал

  эр - Зал электронных ресурсов

  

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