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Труды сотрудников Института органического синтеза УрО РАН - результаты поиска

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Каталог книг и продолжающихся изданий
Сводный каталог иностранных периодических изданий, имеющихся в библиотеках УрО РАН
Сводный каталог отечественных периодических изданий, имеющихся в библиотеках УрО РАН
Каталог диссертаций и авторефератов диссертаций УрО РАН
Каталог препринтов УрО РАН (1975 г. - )
Имидж-каталог отечественных книг (до 2010 г.)
Имидж-каталог иностранных книг (до 2010 г.)
Алфавитно-предметный указатель (АПУ) ЦНБ УрО РАН
Публикации об УрО РАН
Изобретения уральских ученых
Интеллектуальная собственность (статьи из периодики)
Нанотехнологии
Демидовские премии
Гибель династии Романовых
История Урала
Личная библиотека С. В. Вонсовского
Книжная коллекция Шубиных
Труды Института высокотемпературной электрохимии УрО РАН
Труды Института истории и археологии УрО РАН
Труды сотрудников Института горного дела УрО РАН
Труды сотрудников Института органического синтеза УрО РАН
Труды сотрудников Института теплофизики УрО РАН
Труды сотрудников Института химии твердого тела УрО РАН
Расплавы
Труды сотрудников ЦНБ УрО РАН
Публикации Черешнева В.А.
Публикации Чарушина В.Н.
Каталог библиотеки ИЭРиЖ УрО РАН
Электронная энциклопедия «Дискурсология»
Библиометрия
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 1-20    21-34 
1.
Инвентарный номер: нет.
   

   
    Facile synthesis of 6-organyl-4-(trifluoromethyl)pyridin-2(1H)-ones and their polyfluoroalkyl-containing analogs / S. O. Kushch, M. V. Goryaeva, Ya. V. Burgart [et al.] // Russian chemical bulletin. - 2022. - Vol. 71, № 8. - P1687-1700
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The three-component cyclization of 3-polyfluoroalkyl-3-oxopropanoates and methyl ketones with ammonium acetate affords 6-organyl-4-(polyfluoroalkyl)pyridin-2(1H)-ones (organyl is alkyl, aryl, or hetaryl). The synthesized pyridones were evaluated for antifungal, antibacterial, and analgesic activity.

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2.
Инвентарный номер: нет.
   
   S 98

   
    Synthesis and properties of heterocycle-containing podands / E. S. Filatova, O. V. Fedorova, G. L. Rusinov, O. N. Charushin // Chemistry of Heterocyclic Compounds. - 2021. - Vol. 57, № 10. - P971–983
УДК
54
ББК Г
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
HETEROCYCLE-CONTAINING PODANDS -- GLYCOL -- OLIGO(OXYETHYLENE) SPACER -- OPEN-CHAIN ANALOGS OF CROWN ETHERS
Аннотация: The review is devoted to noncyclic analogs of crown ethers (podands) containing an oxyethylene spacer and heterocyclic fragments at one or both of its ends. The paper considers publications on the methods of obtaining and properties of podands for the 2010–2021 period.

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3.
Инвентарный номер: нет.
   
   S 98

   
    Synthesis of novel 3-(pyridin-4-yl)-1,2,4-triazines, their analogs and study of the activity against vaccinia virus / O. V. Shabunina, Y. K. Shtaitz, D. S. Kopchuk [et al.] // Chemistry of Heterocyclic Compounds. - 2021. - Vol. 57, № 4. - P462–466
УДК
Г
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
1,2,4-TRIAZINES -- ANTIVIRAL ACTIVITY -- IPSO SUBSTITUTION -- NUCLEOPHILIC HYDROGEN SUBSTITUTION
Аннотация: Using atom-economical approaches, new representatives of 3-(pyridin-4-yl)-1,2,4-triazines and their 4-nitrophenyl analogs were obtained, and their activity in relation to the vaccinia virus was studied. The new compounds have shown promising characteristics, in particular, in comparison to the antiviral drug Cidofovir.

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4.
Инвентарный номер: нет.
   
   S 83

   
    Stereochemical aspects in the synthesis of novel N-(purin-6-yl)dipeptides as potential antimycobacterial agents / V. V. Musiyak, I. A. Nizova, E. N. Chulakov [et al.] // Amino Acids. - 2021. - Vol. 53, № 3. - P407-415
ББК Г
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
DIPEPTIDES -- RACEMIZATION -- PURINE -- COUPLING -- NUCLEOPHILIC SUBSTITUTION -- ANTIMYCOBACTERIAL ACTIVITY
Аннотация: The synthesis of purine conjugates with natural amino acids is one of the promising directions in search for novel therapeutic agents, including antimycobacterial agents. The purpose of this study was to synthesize N-(purin-6-yl)dipeptides containing the terminal fragment of (S)-glutamic acid. To obtain the target compounds, two synthetic routes were tested. The first of them is based on coupling of N-(purin-6-yl)-(S)-amino acids to dimethyl (S)-glutamate in the presence of carbodiimide coupling agent followed by the removal of ester groups. However, it turned out that this coupling process was accompanied by racemization of the chiral center of N-(purin-6-yl)-α-amino acids and in all cases led to mixtures of (S,S)- and (R,S)diastereomers (6:4). Individual (S,S)-diastereomers were obtained using an alternative approach based on the nucleophilic substitution of chlorine in 6-chloropurine or 2-amino-6-chloropurine with corresponding dipeptides as nucleophiles. The enantiomeric purity of the target compounds was confirmed by chiral HPLC. To test the assumption that racemization of the chiral center of N-(purin-6-yl)-α-amino acids occurs with the participation of nitrogen atoms of the imidazole ring via the stage of formation of a chirally labile intermediate, we obtained such structural analogs of N-(purin-6-yl)-(S)-alanine as N-(9-benzylpurin-6-yl)-(S)-alanine and N-(7-deazapurin-6-yl)-(S)-alanine. It was found that coupling of these compounds to dimethyl (S)-glutamate was also accompanied by racemization. This indicates that the imidazole fragment does not play a crucial role in this process. When testing the antimycobacterial activity of some of the obtained compounds, conjugates with moderate activity against the laboratory Mycobacterium tuberculosis H37Rv strain (MIC 3.1–6.25 μg/mL) were identified.

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5.
Инвентарный номер: нет.
   

   
    The synthesis of aminophenyl-substituted 2,2′-bipyridine ligands by “1,2,4-triazine” methodology / A. P. Krinochkin, D. S. Kopchuk, M. I. Savchuk [et al.] // AIP Conference Proceedings. - 2021. - Vol. 2388, № 1. - Ст. 030016
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: A convenient synthetic approach to the 2,2’-bipyridines, including those with a condensed cyclopentene fragment, having an aminophenyl substituent at the C5 or C6 positions is reported. The products were obtained via their 1,2,4-triazine analogs with a nitro group, by the subsequent transformation of their 1,2,4-triazine ring into a pyridine one and the reduction of the nitro group to the amino group.

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6.
Инвентарный номер: нет.
   

   
    Polyfluoroalkylated antipyrines in Pd-catalyzed transformations / E. V. Shchegolkov, Y. V. Burgart, D. A. Matsneva [et al.] // RSC Advances. - 2021. - Vol. 11, № 56. - P35174-35181
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: In the direct C–H arylation with arylhalogenides in the presence of Pd(OAc)2, trifluoromethyl-containing antipyrine reacts very slowly and incompletely owing to the low nucleophilicity of its C4 center. However, it was effective in modifying polyfluoroalkyl-substituted 4-bromo- and 4-iodo antipyrines by the Suzuki and Sonogashira reactions. It was established that using Pd2(dba)3 as catalyst and XPhos as phosphine ligand was the optimal catalytic system for the synthesis of 4-aryl- and 4-phenylethynyl-3-polyfluoroalkyl-antipyrines. Moreover, iodo-derivatives as the initial reagents were found to be more advantageous compared to bromo-containing analogs. It was found that 4-phenylethynyl-5-CF3-antipyrine has a moderate activity against the influenza virus A/Puerto Rico/8/34 (H1N1) and 4-iodo-5-CF3-antipyrine reveals a weak activity against the vaccine virus (strain Copenhagen) and bovine diarrhea virus (strain VC-1).

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7.
Инвентарный номер: нет.
   

   
    Single-crystal x-ray diffraction studies in a series of 5-pentafluorophenyl-2,2'-bipyridines and their fused analogs / M. V. Varaksin, E. S. Starnovskaya, D. S. Kopchuk [и др.] // Russian journal of general chemistry. - 2020. - Т. 90, № 2. - P235-237
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
6-ARYL-5-PENTAflUOROPHENYL-2,2'-BIPYRIDINES -- LIGANDS -- SINGLE-CRYSTAL X-RAY DIFFRACTION ANALYSIS -- STRUCTURAL EFFECT
Аннотация: Structure of three 6-aryl-5-pentafluorophenyl-2,2'-bipyridines has been studied by means of single-crystal X-ray diffraction analysis. The effect of some functional fragments on the structural organization of compounds, in particular, donor and acceptor substituents in the aryl moiety, as well as annulated benzene and cyclopentane rings on the molecular structure and crystal packing of pentafluorophenyl-modified 2,2'-bipyridine ligand systems has been analyzed.

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8.
Инвентарный номер: нет.
   
   N 39

    Nemytov, A. I.
    SNH methodology in the synthesis of quinazolinap precursors and analogs / A. I. Nemytov, V. A. Ishkhanyan, I. A. Utepova, O. N. Chupakhin // Современные синтетические методологии для создания лекарственных препаратов и функциональных материалов (MOSM2018): вторая международная научно-практическая конференция : материалы и доклады. - Екатеринбург, 2019. - С. 138
ББК Г
Рубрики: ХИМИЧЕСКИЕ НАУКИ

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9.
Инвентарный номер: нет.
   

   
    Synthesis and antioxidant activity of new neomenthyl and caranyl thiotriazoles / Y. V. Gyrdymova, D. V. Sudarikov, S. A. Rubtsova, S. A. Patov, A. V. Kuchin, O. G. Shevchenko, P. A. Slepukhin, F. A. Lakhvich, F. S. Pashkovskii // Chemistry of natural compounds. - 2018. - Vol. 54, № 5. - P883-888
Кл.слова (ненормированные):
TRIAZOLES -- NEOMENTHANE AND CARANE SULFIDES
Аннотация: New neomenthyl and caranyl thiotriazoles were synthesized in up to 80% yields. Studies of the antioxidant and membrane-protective activity of the synthesized compounds in vitro showed that sulfides with a carane moiety were more active than analogs with a neomenthane substituent.

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10.
Инвентарный номер: нет.
   
   D 62

   
    Direct Modification of Quercetin by 6-Nitroazolo[1,5-a]Pyrimidines [Electronic resource] / E. B. Gorbunov, G. L. Rusinov, E. N. Ulomskii, O. S. Eltsov, V. L. Rusinov, V. G. Kartsev, V. N. Charushin, I. A. Khalymbadzha, O. N. Chupakhin // Chemistry of Natural Compounds. - 2016. - Vol. 52, № 4. - С. 708-710
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
DERIVATIVES -- INHIBITORS -- ANALOGS

\\\\expert2\\NBO\\Chemistry of Heterocyclic Compounds\\2016, v.52, N 4, p. 708-710.pdf
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11.
Инвентарный номер: нет.
   
   F 70

   
    Fluorine-containing pyrazoles and their condensed derivatives: Synthesis and biological activity [Electronic resource] / G. N. Lipunova, E. V. Nosova, V. N. Charushin, O. N. Chupakhin // Journal of Fluorine Chemistry. - 2015. - Vol. 175. - С. 84-109. - Bibliogr. : p. 108-109 (119 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
HETEROCYCLIC-COMPOUNDS -- NUCLEOPHILES -- IDENTIFICATION
Аннотация: In the frames of this review article the recently obtained data on new synthetic approaches to fluorinated pyrazoles and their condensed analogs, as well as their biological activities have been analyzed.

\\\\expert2\\nbo\\Journal of Fluorine Chemistry\\2015,V.175, p.84-109.pdf
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12.
Инвентарный номер: нет.
   
   E 97

   
    Exchange Interactions in Cobalt(II) and Nickel(II) Complexes Containing M-4(mu(3)-OH)(2) Metal Cores with Distorted Rhombic Topology [Electronic resource] / A. Golberg, G. G. Aleksandrov, A. S. Bogomyakov, M. A. Kiskin, S. V. Kolotilov, I. A. Utepova, A. A. Sidorov, O. N. Chupakhin, I. L. Eremenko // Theoretical and Experimental Chemistry . - 2015. - Vol. 50, № 6. - С. 364-370. - Bibliogr. : p. 369-370 (21 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
PENTANUCLEAR COMPLEX -- COBALT(II) -- TETRANUCLEAR COMPLEX
Аннотация: Antiferromagnetic interactions between the Co2+ or Ni2+ ions were found in complexes [(mu(3) aEuroaEuro parts per thousand L)(2)Co (5) (II) (mu aEuroaEuro parts per thousand OH)(2)(Piv)(7)(NO3)] and [(mu(3) aEuroaEuro parts per thousand L)(2)(HPiv)Ni (4) (II) (mu(3) aEuroaEuro parts per thousand OH)(2)(Piv)(4)(NO3)(2)] (Piv(-) = pivalic acid anion, L = 1,1'-dipyridazinylferrocene) possessing a metal core with distorted rhombic topology M-4(mu(3)-OH)(2). In contrast to the case of symmetrical analogs, the signs of all the exchange interaction parameters J were determined unambiguously.

\\\\expert2\\nbo\\Theoretical and Experimental Chemistry\\2015, V.50, № 6, p.364-370.pdf
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13.
Инвентарный номер: нет.
   
   F 70

   
    Fluorinated analogs of drugs based on salicylates / E. V. Shchegol'kov, I. V. Shchur, Ya. V. Burgart, V. I. Saloutin, O. P. Krasnykh, L. N. Markova, G. N. Seliverstov // X German-Russian-Ukrainian Symposium on Fluorine Chemistry. - Berlin, 2014. - P. 15
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
SALICYLATES -- DRUGS -- FLUORINATED ANALOGS

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14.
Инвентарный номер: нет.
   
   A 10

   
    A convenient approach to 4,7-dihydrotetrazolo [5,1-c ][1,2,4]triazine synthesis [Electronic resource] / E. V. Shchegol'kov, A. E. Ivanova, Ya. V. Burgart, V. I. Saloutin // Journal of Heterocyclic Chemistry. - 2013. - Vol.50. - PE80-E86
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
TRIAZINE SYNTHESIS -- 1,3-DICARBONYL -- ISOMERISM
Аннотация: Azo coupling of 1,3-dicarbonyl compounds with tetrazolyl-5-diazonium chloride is used to develop a convenient one-step procedure for the synthesis of 4,7-dihydrotetrazolo[5,1-c][1,2,4]triazines. In contrast to nonfluorinated analogs, 7-hydroxy-7-polyfluoroalkyl-4,7-dihydrotetrazolo[5,1-c][1,2,4]triazines undergo a ring-chain isomerism resulting from the cleavage at the C7 - N7a bond. A distinctive feature of nonfluorinated 4,7-dihydrotetrazolo[5,1-c][1,2,4] triazines is the possibility to dehydration, which is accompanied by an azide rearrangement due to the tetrazole ring cleavage with the formation of tetrazolo[1,5-b][1,2,4]triazines

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15.
Инвентарный номер: нет.
   
   S 78

   
    Spin-spin coupling constants 13C-15N and 1H-15N in the investigation of azido-tetrazole tautomerism in a series of 2-azidopyrimidines [Electronic resource] / I. A. Khalymbadzha, T. S. Sheshukova, S. L. Deev , V. L. Rusinov, O. N. Chupakhin, Z. O. Shenkarev, A. S. Arseniev // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2013. - Vol.62, №2. - С. 521-528. - Bibliogr. : p. 528 (25 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
AZIDO-TETRAZOLE EQUILIBRIUM -- SPIN-SPIN COUPLING -- 2-AZIDOPYRIMIDINES
Аннотация: A new method was developed for the investigation of an azido-tetrazole equilibrium based on using a complex analysis of 13C-15N and 1H-15N spin-spin coupling constants. The use of this approach became possible due to the selective inclusion of 15N isotopes into the structures of 2-azidopyrimidines and their cyclic analogs tetrazolo[1,5-a]pyrimidines

\\\\expert2\\nbo\\Russian Chemical Bulletin\\2013, 62 (2), 521-528.pdf
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16.
Инвентарный номер: нет.
   
   F 70

   
    Fluorinated 2-amino-5-phenyl-1,3,4-thiadiazines: synthesis and structures [Electronic resource] / E. V. Shchegol'kov, Ya. V. Burgart, V. I. Saloutin, O. N. Chupakhin // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2013. - Vol.62, №1. - С. 220-222
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
THIADIAZINES -- TAUTOMERIC STRUCTURES -- 4H-TAUTOMER
Аннотация: Fluorinated 2-amino-5-phenyl-1,3,4-thiadiazines were obtained for the first time. A study of their tautomeric structures revealed that trifluoromethyl-containing 1,3,4-thiadiazines exist as the 4H-tautomer in both solutions and the solid state, while their monofluoroaryl analogs exist as the 6H-tautomer

\\\\expert2\\nbo\\Russian Chemical Bulletin\\2013, 62 (2), 521-528.pdf
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17.
Инвентарный номер: нет.
   
   F 33

   
    Features of the reaction of 3(5)-methyl-5(3)-trifluoromethylpyrazole with chloroform. Synthesis and structure of fluorinated analogs of tris(pyrazol-1-yl)methane / N. S. Boltacheva, P. A. Slepukhin, M. G. Pervova, M. A. Samorukova, L. G. Lavrenova, V. I. Filyakova, V. N. Charushin // Russian Journal of General Chemistry. - 2012. - Vol.82, №8. - С. 1444-1450
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
CHLOROFORM -- TRIFLUOROMETHYLPYRAZOLE -- TRIS(PYRAZOL-1-YL)METHANE
Аннотация: Reaction of 3(5)-methyl-5(3)-trifluoromethylpyrazole (I) with chloroform leads to a complex mixture of compounds. The main components are {bis[(5-methyl-3-trifluoromethyl)pyrazol-1-yl](3-methyl-5-trifluoromethyl)pyrazol-1-yl}methane, bis{[(3-methyl-5-trifluoromethyl)pyrazol-1-yl](5-methyl-3-trifluoromethyl)-pyrazol-1-yl}methane, and tris[(3-methyl-5-trifluoro-methyl)pyrazol-1-yl]methane. The structure of isomeric substances was proved by XRD method

\\\\Expert2\\nbo\\Russian Journal of General Chemistry\\2012, V. 82, N 8, p. 1444–1450.pdf
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18.
Инвентарный номер: нет.
   
   D 44

   
    Deprotonation of pyrazole and its analogs by aqueous copper acetate in the presence of triethylamine / M. A. Yakovleva , E. V. Kushan, N. S. Boltacheva, V. I. Filyakova, S. E. Nefedov // Russian Journal of Inorganic Chemistry (Zhurnal Neorganicheskoi Khimii). - 2012. - Vol. 57, № 2. - С. 181-192
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
SECONDARY BUILDING UNITS -- MAGNETIC-PROPERTIES -- COORDINATION POLYMERS
Аннотация: Deprotonation reactions of pyrazole and its analogs by aqueous copper acetate in benzene at room temperature in the presence of triethylamine were studied. Unlike 3,5-dimethylpyrazole, more acidic pyrazole, 5-methyl-3-trifluoromethylpyrazole, and 3,5-bis(trifluoromethyl)pyrazoles are deprotonated to give pyrazolate bridges. The structural features of the obtained compounds are discussed based on X-ray diffraction data

\\\\Expert2\\nbo\\Russian Journal of Inorganic Chemistry\\2012, v. 57, N. 2, p.181-192.pdf
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19.
Инвентарный номер: нет.
   
   C 51

   
    Chemoselectivity in the Reduction of (2S,4S)-4-Amino-5-oxoproline Derivatives with Borane Complexes [Text] / A. Yu. Vigorov, I. A. Nizova, L. Sh. Sadretdinova, M. A. Ezhikova, M. I. Kodess, I. N. Ganebnuikh, V. P. Krasnov // European Journal of Organic Chemistry. - 2011. - № 13. - P2562-2569. - Bibliogr. : p. 2569 (21 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Reduction of the carbonyl groups in N-protected (2S,4S)-4-amino- 5-oxo-1-phenylprolinates with BH(3) complexes resulted in (2S,4S)-4-aminoproline or (2S,4S)-4-aminoprolinol derivatives depending on the reaction conditions and the type of protecting groups used

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20.
Инвентарный номер: нет.
   
   S 98

   
    Synthesis and antiviral activity of nucleoside analogs based on 1,2,4-triazolo[3,2-c][1,2,4]triazin-7-ones [Electronic resource] / V. L. Rusinov, O. N. Chupakhin, S. L. Deev, T. S. Shestakova, E. N. Ulomskii, L. I. Rusinova, O. I. Kiselev, E. G. Deeva // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2010. - Vol. 59, № 1. - P136-143
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
NUCLEOSIDE ANALOGS -- ANTIVIRAL DRUGS -- HYDROXYETHOXYMETHYL
Аннотация: Nucleoside analogs containing hydroxybutyl, hydroxyethoxymethyl, allyloxymethyl, and propargyloxymethyl fragments were synthesized based on 1,2,4-triazolo[3,2-c][1,2,4]triazin-7-ones isosteric to purine bases. Some of the compounds obtained inhibit in vitro reproduction of influenza and respiratory syncytial virus infection

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2010, 59 (1), 136-143.pdf
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  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

  

Сиглы библиотек институтов и НЦ УрО РАН
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