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Каталог книг и продолжающихся изданий
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Труды Института высокотемпературной электрохимии УрО РАН
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Труды сотрудников Института горного дела УрО РАН
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Труды сотрудников ЦНБ УрО РАН
Публикации Черешнева В.А.
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Каталог библиотеки ИЭРиЖ УрО РАН
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1.
Инвентарный номер: нет.
   
   П 50

   
    Полифторбензоилхлориды и изотиоцианаты в реакциях с СH-активными бензимидазолами [] = Polyfluorobenzoyl chlorides and isothiocyanates in reactions with CH-reactive benzimidazoles / Э. В. Носова, Г. Н. Липунова, А. А. Лаева, В. Н. Чарушин // Изв. АН. Сер. Химическая. - 2005. - N 3. - 720-724: рис. - Библиогр. : с. 724 (24 назв.) . - ISSN 0002-3353
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Взаимодействием (2-бензоилметил)бензимидазола с тетра- и пентафторбензоилхлоридами получены фторсодержащие 6-бензоил-7H-бензимидазо[3,2-а]хинолоны. На основе 2-цианометилбензимидазола или 2-бензоилметилбензимидазола и тетра(пента)фторбензоилизотиоцианатов синтезированы фторсодержащие 1,3-бензотиазиноны, для которых выявлены различия в реакциях с циклоалкилиминами.

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2.
Инвентарный номер: нет.
   
   S 98

   
    Synthesis of fluoroalkyl-containing 1,2,3-triketone 2-hetarylhydrazones and their reactions with hydrazines [Electronic resource] / E. V. Shchegol'kov, Ya. V. Burgart, O. G. Khudina, V. I. Saloutin, O. N. Chupakhin // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2004. - Vol. 53, № 11. - P2584-2590
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Fluoroalkyl-containing 1,2,3-triketone 2-(2,3-dimethyl-5-oxo-1-phenyl-1,2-dihydropyrazol-4-yl)-, 2-(4-ethoxycarbonylpyrazol-3-yl)-, and 2-(1,2,4-triazol-3-yl)hydrazones were synthesized by the azo coupling reactions of fluorinated 1,3-diketones with the corresponding hetaryldiazonium chlorides. The hetarylhydrazones thus synthesized were subjected to cyclocondensation with hydrazines at the 1,3-dicarbonyl fragment to give 3-fluoroalkyl-4-hetarylazopyrazoles

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2004, 53 (11), 2584-2590.pdf
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3.
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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4.
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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5.
Инвентарный номер: нет.
   
   S 98

   
    Synthesis of Assemblies of Isoxazole and Azoles Based on 1,3-Dipolar Cycloaddition Reaction of Enamines with Nitrile Oxides = Cинтез ансамблей изоксазолов c азолами в реакции 1,3-диполярного циклоприсоединения енаминов к нитрилоксидам / I. Efimov, Yu. Shafran, N. N. Volkova, N. Beliaev, P. A. Slepukhin, V. A. Bakulev // Chemistry of Heterocyclic Compounds. - 2016. - Vol. 52, № 9. - С. 743-749. - Bibliogr. : p. 748-749 (32 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
ENAMINES -- ISOXAZOLES -- HYDROXAMOYL CHLORIDES
Аннотация: 2-(1,2,3-Thiadiazol-5-yl)enamines and 3-(1,2,3-triazol-4-yl)enaminones react with arylhydroxamoyl chlorides at room temperature with the exclusive formation of 3-aryl-4-(1,2,3-thiadiazol-5-yl)- and [4-(1,2,3-triazol-4-yl)carbonyl]isoxazoles in high yields. The proposed mechanism includes in situ generation of nitrile oxides, which participate in the (3+2)-dipolar cycloaddition reactions leading to the formation of the isoxazole ring.

\\\\expert2\\NBO\\Chemistry of Heterocyclic Compounds\\2016, v.52, N 9, p. 743-749.pdf
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6.
Инвентарный номер: нет.
   
   S 98

   
    Synthesis of 5-and 7-fluoroquinazolin-4(1H)-ones [Electronic resource] / A. A. Layeva, E. V. Nosova, G. N. Lipunova, T. V. Trashakhova, V. N. Charushin // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2007. - Vol. 56, № 9. - P1821-1827
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: 5-Fluoroquinazoline-2,4-diones and their 2-thio analogs were obtained from 6-fluoroanthranilic acid. Two convenient routes to 5-fluoroquinazolin-4-ones involved cyclocondensation of 6-fluoroanthranilamide with acid chlorides (anhydrides) or with aromatic (heterocyclic) aldehydes. A method for the synthesis of 7-fluoroquinazolin-4-one from 2,4-difluorobenzoic acid was proposed

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2007, 56 (9), 1821.pdf
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7.
Инвентарный номер: нет.
   
   K 96

    Kuzueva, O. G.
    Synthesis of 2-arylhydrazones of aliphatic fluorine-containing 1,2,3-tricarbonyl compounds and their reactions with dinucleophiles [Electronic resource] / O. G. Kuzueva, Ya. V. Burgart, V. I. Saloutin // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 1998. - Vol. 47, № 4. - P673-678
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: New fluorinated 2-arylhydrazones of 1,2,3-tricarbonyl compounds were obtained by coupling fluorine-containing 3-oxo esters, 1,3-diketones, and their copper chelates with aryldiazonium chlorides. Reactions of these arylhydrazones with hydrazine hydrate, phenylhydrazine, thiosemicarbazide, and hydroxylamine gave the corresponding pyrazole and isoxazole derivatives

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\1998, 47 (4), 673.pdf
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8.
Инвентарный номер: нет.
   
   S 98

   
    Synthesis and the reactions of trifluoromethylated 1,2,3-triketones 2-(het)arylhydrazones and 4,7-dihydroazolo[5,1-c]triazines [Electronic resource] / O. G. Khudina, E. V. Shchegol'kov, Ya. V. Burgart, M. I. Kodess, O. N. Kazheva, A. N. Chekhlov, G. V. Shilov, O. A. Dyachenko, V. I. Saloutin, O. N. Chupakhin // Journal of Fluorine Chemistry. - 2005. - Vol. 126, № 8. - P1230-1238
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The coupling of trifluoromethylated 1,3-diketones with (het)aryldiazonium chlorides results mainly in the formation of 1,2,3-triketones 2-(het)arylhydrazones while using hetarylamine with a NH-group at the ?-position of the heterocycle as the diazonium component gives 4,7-dihydroazolo[5,1-c]triazines due to cyclization at the trifluoroacetyl fragment. Trifluoromethylated 1,2,3-triketones 2-(het)arylhydrazones and 7-hydroxy-4,7-dihydroazolo[5,1-c]triazines react regio-selectively with methyl hydrazine and phenyl hydrazine to form 3-CF3-pyrazoles. The long-range coupling constants (JF-H) of 1-methylpyrazoles and the chemical shifts of trifluoromethyl groups in the 19F NMR spectra can be used for the determination of regio-isomeric structures of mono(trifluoromethyl)-substituted pyrazoles. 2-(Het)arylhydrazones and 4,7-dihydroazolo[5,1-c]triazines with two trifluoromethyl substituents afford the mixtures of cis- and trans-azopyrazoles in the reactions with hydrazines.

\\\\Expert2\\nbo\\Journal of Fluorine Chemistry\\2005, v.126, p.1230.pdf
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9.
Инвентарный номер: нет.
   
   S 91

   
    Substituent effect on the stereoselectivity of acylation of racemic heterocyclic amines with N-phthaloyl-3-aryl-(S)-alanyl chlorides [Text] / G. L. Levit, D. A. Gruzdev, V. P. Krasnov, E. N. Chulakov, L. Sh. Sadretdinova, M. A. Ezhikova, M. I. Kodess, V. N. Charushin // Tetrahedron: Asymmetry . - 2011. - Vol. 22, № 2. - P185-189. - Bibliogr. : p. 189 (17ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The acylative kinetic resolution of racemic 2-methyl-1,2,3,4-tetrahydroquinoline and 2,3-dihydro-3-methyl-4H-1,4-benzoxazine using acyl chlorides of N-phthaloyl-(S)-phenylalanine, N-phthaloyl-3-(4-nitrophenyl)-(S)-alanine and N-phthaloyl-O-methyl-(S)-tyrosine as chiral resolving agents has been carried out. It is shown that the effectiveness of an acylative kinetic resolution depends on the electronic effects of substituents in the phenyl fragment of the acylating agent and increases as the electron-donating properties of the para-substituent (OMe H NO2) in phenyl fragment of N-phthaloyl-3-aryl-(S)-alanyl chlorides increase; conducting the process at a reduced temperature also contributes to an enhancement of the kinetic resolution

\\\\Expert2\\nbo\\Tetrahedron Asymmetry\\2011, v. 22, p.185.pdf
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10.
Инвентарный номер: нет.
   
   S 89

   
    Structure of diethyl (polyfluorobenzoyl)malonates and their thermal intramolecular cyclizat / D. N. Bazhin, E. V. Schegolkov, Yu. S. Kudyakova, Ya. V. Burgart, V. I. Saloutin // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2011. - Vol.60, №5. - С. 929-932
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
POLYFLUOROBENZOYL -- POLYFLUOROBENZOYL CHLORIDES -- CYCLIZATION
Аннотация: The reaction of the C-ethoxymagnesium derivative of diethyl malonate with polyfluorobenzoyl chlorides affords the corresponding (polyfluorobenzoyl)malonates prone to thermal cyclization into coumarin derivatives. The compounds obtained are inherent in keto—enol tautomerism

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2011, 60 (5), 929-932.pdf
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11.
Инвентарный номер: нет.
   
   R 30

   
    Reactivity of 1,2,3-triazoles towards sulfonyl chlorides. A novel approach to 1-and 2-sulfonyl-4-azolyl-1,2,3-triazoles / T. Beryozkina, I. Efimov, W. M. F. Fabian, N. Beliaev, P. A. Slepukhin, M. L. Isenov, W. Dehaen, G. Lubec, O. S. Eltsov, Z. Fan // Tetrahedron. - 2015. - Vol. 71, № 36. - С. 6189-6195
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
1,2,3-TRIAZOLES -- SULFONYL CHLORIDES -- 2-SULFONYL-4-AZOLYL-1,2,3-TRIAZOLES

\\\\expert2\\NBO\\Tetrahedron\\2015, v. 71 , p. 6189.pdf
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12.
Инвентарный номер: нет.
   
   P 80

   
    Polyfluorobenzoyl chlorides and isothiocyanates in reactions with CH-reactive benzimidazoles [Electronic resource] / E. V. Nosova, G. N. Lipunova, A. A. Laeva, V. N. Charushin // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2005. - Vol. 54, № 3. - P733-737
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Reactions of 2-benzoylmethylbenzimidazole with tetra- and pentafluorobenzoyl chlorides afford fluorine-containing 6-benzoyl-7H-benzimidazo[3,2-a]quinolones. 2-Cyanomethyl- or 2-benzoylmethylbenzimidazole reacts with tetra(penta) fluorobenzoyl isothiocyanates to give fluorine containing 1,3-benzothiazinones, which differently behave in reactions with cycloalkylimines

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2005, 54 (3), 733.pdf
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13.
Инвентарный номер: нет.
   
   N 89

   
    Novel 3-acetyl-2-methyl-polyfluorochromones in reactions with amines and esters of amino acids [Electronic resource] / K. V. Shcherbakov, D. N. Bazhin, Ya. V. Burgart, V. I. Saloutin // Chemistry of Heterocyclic Compounds. - 2015. - Vol. 51, № 11/12. - С. 961-968. - Bibliogr. : p. 967-968 (21 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
AMINE -- ACYLATION -- CHROMONE
Аннотация: Novel 3-acetyl-2-methyl-polyfluoro-4Н-chromen-4-ones were obtained via one-pot acylation of acetylacetone with polyfluorobenzoyl chlorides. These chromones were shown to form N-substituted 3-amino-1-[2-hydroxy(polyfluoro)phenyl]but-2-en-1-ones in reaction with aliphatic primary amines, esters of amino acids, and aqueous ammonia via opening of the pyrone ring and deacylation

\\\\expert2\\nbo\\Chemistry of Heterocyclic Compounds\\2015, v.51, N 11-12, p. 961-968.pdf
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14.
Инвентарный номер: нет.
   
   K 49

    Kisil', S. P.
    New Fluoroaryl-containing beta,beta'-Dioxoesters in the Synthesis of Fluorobenzopyran-2(4)-ones [Electronic resource] / S. P. Kisil', Ya. V. Burgart, V. I. Saloutin // Russian Journal of Organic Chemistry (Translation of Zhurnal Organicheskoi Khimii). - 2001. - Vol. 37, № 10. - P1455-1462
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: For the first time were obtained ethyl 2-(2-methoxy-3,4,5,6-tetrafluorobenzoyl)-3-oxobutanoate and ethyl 2-pentafluorobenzoyl-3-oxobutanoate and their copper chelates. The compounds were prepared by acylation of ethyl acetoacetate with 2-methoxy-3,4,5,6-tetrafluoro- and pentafluorobenzoyl chlorides. Cyclization of these ,'-dioxoesters afforded substituted chromones. 2-Methyl-5-methoxy-6,7,8-trifluoro-3-ethoxycarbonylchromone hydrolyzes depending on reaction conditions either to 5-hydroxy-2-methyl-6,7,8-trifluorochromone or to 5-hydroxy-2-methyl-6,7,8-trifluorochromone-3-carboxylic acid. Reaction with morpholine provided 7-substituted product, and with aqueous ammonia as a result of rearrangement forms 3-acetimidoyl-4-hydroxy-5-methoxy-6,7,8-trifluorocoumarin. Hydrolysis of the latter yields 3-acetyl-4-hydroxy-5-methoxy-6,7,8-triflu

\\\\Expert2\\nbo\\Russian Journal of Organic Chemistry\\2001, 37 (10), 1455.pdf
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15.
Инвентарный номер: нет.
   
   N 10

   
    N-heterocyclic carbenes. IV.(1)Synthesis of symmetrical and unsymmetrical imidazolium salts with abietane moiety / V. A. Glushkov, K. A. Arapov, M. S. Kotelev, K. S. Rudowsky, K. Yu. Suponitsky, A. A. Gorbunov, O. A. Maiorova, P. A. Slepukhin // Heteroatom Chemistry. - 2012. - Vol.23, №1. - С. 5-15
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
IMIDAZOLINIUM -- 12-AMINODEHYDROABIETATE -- SALTS OF IMIDAZOLINIUM
Аннотация: Methyl 12-chloromethyl-dehydroabie-tate reacts with 1-benzyl- and 1-arylimidazoles to give unsymmetrically substituted imidazolium chlorides (1a–i), with abietane moiety. Starting from methyl 12-aminodehydroabietate, symmetrically substituted diterpene-based salts of imidazolinium (4) and imidazolium (5) were synthesized. Anion exchange afforded corresponding (1e·BF4) and (1e·PF6). The new compounds were tested as ligands for a Pd-catalyzed Suzuki-Miyaura reaction. The molecular structure of (1e) is reported

\\\\Expert2\\nbo\\Heteroatom Chemistry\\2012, V. 23, N 1, P. 5-15.pdf
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16.
Инвентарный номер: нет.
   

   
    Mutual kinetic resolution of 3-methyl-3,4-dihydro-2h-1,4-benzoxazines and 2-alkoxyacyl chlorides / S. A. Vakarov, D. Gruzdev, L. S. Sadretdinova, M. I. Kodess, A. A. Tumashov, E. B. Gorbunov, G. L. Levit, V. P. Krasnov // Chemistry of Heterocyclic Compounds. - 2018. - Vol. 54, № 4. - P437-446
Рубрики: ХИМИЧЕСКИЕ НАУКИ

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17.
Инвентарный номер: нет.
   
   K 46

   
    Kinetic resolution of racemic 6-substituted 1,2,3,4-tetrahydroquinaldines with chiral acyl chlorides. Experiment and quantum chemical simulation / E. N. Chulakov, M. A. Korolyova, L. S. Sadretdinova [et al.] // Russian chemical bulletin. - 2021. - Vol. 70, № 5. - P890-899
ББК Г
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: A comparative study of the kinetic resolution (KR) of racemic 6-substituted 2-methyl-1,2,3,4-tetrahydroquinolines with acyl chlorides of (S)-naproxen, N-phthaloyl-(S)-leucine, and (R)-O-phenyllactic acid was carried out. The selectivity factors in the KR of racemic amines with acyl chlorides of (S)-naproxen and (R)-O-phenyllactic acid were shown to be approximately the same and higher than those for the KR of N-phthaloyl-(S)-leucyl chloride. The reasons for the stereodifferentiation in the KR of racemic tetrahydroquinaldines containing groups of different electronic properties by acyl chlorides of three different chiral acids were explained using the DFT method. The conditions for stabilizing π—π interactions of aromatic fragments of the reagents, which do not occur in the same form in the transition state and lead to the minor diastereoisomeric product, are created in the transition state of the faster acylation reaction with (S)-naproxen and (R)-O-phenyllactic acyl chlorides. In the case of the KR of 2-methyl-1,2,3,4-tetrahydroquinoline and 2-methyl-6-methoxy-1,2,3,4-tetrahydroquinoline with N-phthaloyl-(S)-leucyl chloride, the acylation diastereoselectivity is determined, most likely, by conformational factors. The individual (S)-enantiomer of 2-methyl-6-methoxy-1,2,3,4-tetrahydroquinoline of high optical purity was synthesized using the KR of the racemate with (S)-naproxen acyl chloride.

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18.
Инвентарный номер: нет.
   
   K 46

   
    Kinetic resolution of heterocyclic amines by reaction with optically active acid chlorides. The effect of reaction conditions on the diastereoselectivity of acylation of (±)-3-methyl-2,3-dihydro-4H-1,4-benzoxazine [Electronic resource] / V. P. Krasnov, G. L. Levit, M. A. Koroleva, I. M. Bukrina, L. Sh. Sadretdinova, I. N. Andreeva, V. N. Charushin, O. N. Chupakhin // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2004. - Vol. 53, № 6. - P1253-1256
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The influence of the reaction conditions (solvent, base) on the diastereoselectivity of acylation of (±)-3-methyl-2,3-dihydro-4H-1,4-benzoxazine with (S)-naproxen and N-tosyl-(S)-proline chlorides was studied. The highest diastereoselectivity was observed for the reaction carried out in benzene in the presence of aliphatic tertiary amines

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2004, 53 (6), 1253.pdf
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19.
Инвентарный номер: нет.
   
   K 46

   
    Kinetic resolution of 1-methyl- and 1-phenyl-3-amino-1,2-dicarba-closo-dodecaboranes via acylation with chiral acyl chlorides [Electronic resource] / G. L. Levit, V. P. Krasnov, A. M. Demin, M. I. Kodess, L. Sh. Sadretdinova, T. V. Matveeva, V. A. Ol'shevskaya, V. N. Kalinin, O. N. Chupakhin, V. N. Charushin // Mendeleev Communications. - 2004. - Vol. 14, № 6. - P293-295
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: A study of the kinetic resolution of racemic 1-substituted 3-amino-1,2-dicarba-closo-dodecaboranes by chiral acyl chlorides has shown that N-tosyl-(S)-prolyl and N-phthaloyl-(S)-alaninyl chlorides are more efficient resolving agents than (S)-naproxen chloride.

\\\\Expert2\\nbo\\Mendeleev Communications\\2004, v.14, p.293.pdf
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20.
Инвентарный номер: нет.
   
   K 46

   
    Kinetic resolution of (±)-2,3-dihydro-3-methyl-4h-1,4-benzoxazines with (s)-naproxen / V. N. Charushin, V. P. Krasnov, G. L. Levit, M. A. Koroleva, M. I. Kodess, O. N. Chupakhin, M. N. Kim, H. S. Lee, Y. J. Park, K. -C. Kim // Tetrahedron: Asymmetry . - 1999. - Vol. 10, № 14. - С. 2691-2702. - Bibliogr. : p. 2702 (13 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
ENANTIOMERS -- BENZOXAZINES -- ACYL CHLORIDES

\\\\Expert2\\nbo\\Tetrahedron Asymmetry\\1999. v. 10. p.2691.pdf
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