Центральная Научная Библиотека УрО РАН

Вид документа : Статья из журнала
Шифр издания : 54/N 89
Автор(ы) : Saloutin V. I., Skryabina Z. E., Bazyl I. T., Chupakhin O. N.
Заглавие : Novel fluorinated chromones
Место публикации : Journal of Fluorine Chemistry. - 1993. - Vol. 65, N 1-2. - С. 37-41
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The self-condensation of ethyl pentafluorobenzoylacetate leads to the formation of 3-pentafluorophenyl-1H-sopyrono[2,3-b]-6,7,8,9-tetrafluorochrom in 37% yeld. On hydrolysis, this gave 2-pentafluorobenzoylmethyl-5,6,7,8-tetrafluorochromone
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Вид документа : Статья из журнала
Шифр издания : 54/S 98
Автор(ы) : Krasnov V. P., Nizova I. A., Sinitsyna T. A., Avdyukova N. V.
Заглавие : Synthesis and study of (2S, 4S)-4-arylamino-2-carboxy-5-pyrrolidones [Electronic resource]
Место публикации : Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 1993. - Vol. 42, № 12. - С. 2001-2004
Систем. требования: http://www.springerlink.com/content/lq72342137q275rh/fulltext.pdf
Примечания : 21.10.2011
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: (2S, 4S)-4-Arylamino-2-carboxy-5-pyrrolidones were prepared by hydrolysis of dimethyl (2S, 4S)-4-arylamino-N-phthaloylglutamates. The protonation constants of the arylamino group in the synthesized compounds were determined.
\\\\Expert2\\nbo\\Russian Chemical Bulletin\\1993, 42 (12), 2001-2004.pdf
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Вид документа : Статья из журнала
Шифр издания : 54/H 99
Автор(ы) : Bazhenova L. N., Filyakova V. I., Kirichenko V. E., Pashkevich K. I.
Заглавие : Hydrolysis of fluoroalkyl-containing beta-aminovinyl ketones [Electronic resource]
Место публикации : Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 1991. - Vol. 40, N 3. - С. 581-585
Систем. требования: http://www.springerlink.com/content/jv305g3763282610/fulltext.pdf
Примечания : 21.10.2011
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
\\\\Expert2\\nbo\\Russian Chemical Bulletin\\1991, 40 (3), 581.pdf
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Вид документа : Статья из журнала
Шифр издания : 54/T 64
Автор(ы) : Shishmakov A. B., Mikushina Yu. V., Valova M. S., Koryakova O. V., Petrov L. A.
Заглавие : Titanium dioxide xerogel modified with powder cellulose in oxidation of trimethylhydroquinone [Electronic resource]
Место публикации : Russian Journal of Applied Chemistry. - 2007. - Vol. 80, № 12. - С. 2107-2110
Систем. требования: http://www.springerlink.com/content/g263472857628tm3/fulltext.pdf
Примечания : Библиогр. : с. 2110 (17 назв.). - 19.10.2011
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: A procedure was developed for modification of titanium dioxide xerogel by addition of powder cellulose in the stage preceding hydrolysis of tetramethoxytitanium. The resulting catalytic systems based on the new material were studied in a model liquid-phase catalytic process of oxidative dehydrogenation of trimethylhydroquinone with atmospheric oxygen.
\\\\Expert2\\nbo\\Russian Journal of Applied Chemistry\\2007, v. 80, N 12, p.2107.pdf
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Вид документа : Статья из журнала
Шифр издания : 54/A 18
Автор(ы) : Levit G. L., Demin A. M., Kodess M. I., Ezhikova M. A., Sadretdinova L. Sh., Ol'shevskaya V. A., Kalinin V. N., Krasnov V. P., Charushin V. N.
Заглавие : Acidic hydrolysis of N-acyl-1-substituted 3-amino-1,2-dicarba-closo-dodecaboranes
Место публикации : Journal of Organometallic Chemistry. - 2005. - Vol. 690, № 11. - С. 2783-2786
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Acidic hydrolysis of N-acyl 1-methyl- and 1-phenyl-3-amino-1,2-dicarba-closo-dodecaboranes has been studied. It has been shown that acidic hydrolysis of diastereomeric amides of 1-methyl-3-amino-1,2-dicarba-closo-dodecaborane results in the partial racemization of the target 3-amino-1-methylcarborane. Under the similar conditions, the hydrolysis of N-acyl-3-amino-1-phenyl-1,2-dicarba-closo-dodecaboranes resulted in amide bond cleavage accompanied by simultaneous deboronation with the removal of boron atom at position 6 of carborane cage and formation of 7,8-dicarba-nido-undecaborane derivative according to 11B and 1H NMR spectroscopy.
\\\\Expert2\\nbo\\Journal of Organometallic Chemistry\\2005, v. 690, p.2783.pdf
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Вид документа : Статья из журнала
Шифр издания : 54/T 44
Автор(ы) : Medvedeva N., Polyak Yu., Kuzikova I., Orlova O., Zharikov G.
Заглавие : The effect of mustard gas on the biological activity of soil
Место публикации : Environmental Research. - 2008. - Vol. 106, № 3. - С. 289-295
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: A special group of substances that are very dangerous for the biosphere includes war gases such as mustard gas (bis(2-chloroethyl)sulphide). The influence of mustard gas hydrolysis products (MGHPs) on soil microbiota has been investigated. These substances bear numerous toxic effects on soil microorganisms. They change significantly the number and the specific composition of soil microbiota and inhibit the enzyme activity of soils. The main "ecological targets" of mustard and its hydrolysis products' toxic action have been determined. MGHPs affect the growth and reproduction of soil micromycetes, as well as their morphological and cultural properties. Increase in number and size of mitochondria in the fungal cells is accompanied by increase in dehydrogenases activity. Cell permeability influenced by MGHPs grows in connection with concentration of toxicants. Increase of permeability corresponds to growth of the amount of unsaturated fatty acids. The changes in the fatty acid composition of lipids in the cells of the soil micromycetes display their adaptation to adverse impact of the substances studied. MGHPs and thiodiglycol enhance synthesis of polysaccharides and pigments.
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Вид документа : Статья из журнала
Шифр издания : 54/S 89
Автор(ы) : Krasnov V. P., Nizova I. A., Vigorov A. Yu., Matveeva T. V., Levit G. L., Slepukhin P. A., Ezhikova M. A., Kodess M. I.
Заглавие : Structure and properties of 4-amino derivatives of 5-oxoproline
Место публикации : European Journal of Organic Chemistry. - 2008. - № 10. - С. 1802-1810
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: On the basis of the results obtained from NMR spectroscopy, X-ray analysis and chemical transformations, it was established that acidic hydrolysis of (2S,4S)-4-arylaminoglutamates results in the formation of lactams in which ring closure occurs with the participation of the Y-amino and alfa-COOH groups; but isomeric lactams resulting from the participation of the alfa-amino and Y-COOH groups are not formed. Isomeric lactams, that is, (2S,4S)-4-arylamino-5-oxoprolines, can be easily converted in acidic medium into more stable 4-amino-1-aryl-5-oxoprolines.
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Вид документа : Статья из журнала
Шифр издания : 54/S 98
Автор(ы) : Fokin A. S., Burgart Ya. V., Saloutin V. I., Chupakhin O. N.
Заглавие : Synthesis of fluorine-containing 2-(1-aryl-4-oxo-1,4-dihydrocinnolin-3-yl)-2-oxoacetic acids [Electronic resource]
Место публикации : Russian Journal of Organic Chemistry (Translation of Zhurnal Organicheskoi Khimii). - 2005. - Vol. 41, № 9. - С. 1374-1376
Систем. требования: http://www.springerlink.com/content/7220j35k2t7qr690/fulltext.pdf
Примечания : Библиогр. : с. 1376 (9 назв.). - 28.10.2011 г.
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Acid hydrolysis of ethyl 2-(1-aryl-5,6,7,8-tetrafluoro-4-oxo-1,4-dihydrocinnolin-3-yl)-2-oxoacetates gives 2-(1-aryl-5,6,7,8-tetrafluoro-4-oxo-1,4-dihydrocinnolin-3-yl)-2,2-dihydroxyacetic acids which undergo dehydration on heating in toluene to afford 2-(1-aryl-5,6,7,8-tetrafluoro-4-oxo-1,4-dihydrocinnolin-3-yl)-2-oxoacetic acids. Reactions of the latter with excess morpholine result in replacement of two fluorine atoms in positions 5 and 7 by the amine residues.
\\\\Expert2\\nbo\\Russian Journal of Organic Chemistry\\2005, 41 (9), 1374-1376.pdf
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Вид документа : Статья из журнала
Шифр издания : 54
Автор(ы) : Ratner V. G., Lork E., Pashkevich K. I., Roeschenthaler G.-V.
Заглавие : (E)-1,1,1-trifluoro-4-phenyl-but-2-ene-4-one and trimethyl phosphite
Место публикации : Journal of Fluorine Chemistry. - 2000. - Vol. 102, № 1-2. - С. 73-77
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The interaction of (E)-1,1,1-trifluoro-4-phenyl-but-2-ene-4-one (1) with trimethyl phosphite affords in a [4 + 1] cycloaddition the 1,2?5-oxaphospholene 2 as a sole product which upon hydrolysis is transformed into the fluoroalkyl containing ?-ketophosphonate 4. When the reaction is carried out in the presence of small mounts of water, in addition to 2 as a main product, the phosphoric acid ester 6 of the enolic dimer of ketone 1 is also formed. The molecular structure of compound 6 (monoclinic P 2(1)/c with a = 2088.60(2), b = 1403.1(3), c = 1613.8(1) pm, ? = 90, ? = 100.97(1), ? = 90°, Z = 8) was determined, indicating two independent molecules with (RR) and (SS) configuration and disordered CF3 groups.????
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10.

Вид документа : Статья из журнала
Шифр издания : 54/F 70
Автор(ы) : Kisil' S. P., Burgart Ya. V., Saloutin V. I., Chupakhin O. N.
Заглавие : Fluoroaryl containing beta,beta-dioxoesters in the synthesis of fluorobenzopyran-4(2)-ones
Место публикации : Journal of Fluorine Chemistry. - 2001. - Vol. 108, № 2. - С. 125-131
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Fluoroaryl containing ?,??-dioxoesters and their copper(II) chelates have been prepared by acylation of ethyl acetoacetate with 2,6-dimethoxy-3,4,5-trifluorobenzoyl, 2-methoxy-3,4,5,6-tetrafluorobenzoyl and pentafluorobenzoyl chlorides. Cyclization of these ?,??-dioxoesters leads to formation of substituted fluorochromones. Depending on conditions, 2-methyl-5-methoxy-6,7,8-trifluoro-3-ethoxycarbonylchromone hydrolyzed to 5-hydroxy-2-methyl-6,7,8-trifluorochromone or 5-hydroxy-2-methyl-6,7,8-trifluorochromone-3-carboxylic acid. The same chromone reacts with morpholine to form a seven-substituted product and ammonium hydroxide to give 3-iminoacetyl-4-hydroxy-5-methoxy-6,7,8-trifluorocoumarin. Hydrolysis of the latter affords 3-acetyl-4-hydroxy-5-methoxy-6,7,8-trifluorocoumarin. Ethyl-2-(2,6-dimethoxy-3,4,5-trifluorobenzoyl)-3-oxobutanoates undergoes ketone-splitting to 1-(2,6-dimethoxy-3,4,5-trifluorophenyl)-1,3-butandione????
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11.

Вид документа : Статья из журнала
Шифр издания : 54/E 54
Автор(ы) : Krasnov V. P., Levit G. L., Charushin V. N., Kodess M. I., Kalinin V. N., Chupakhin O. N.
Заглавие : Enantiomers of 3-amino-1-methyl-1,2-dicarba-closo-dodecaborane
Место публикации : Tetrahedron: Asymmetry . - 2002. - Vol. 13, № 16. - С. 1833-1835
Примечания : Bibliogr. : p. 1835 (6 ref.)
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The enantiomers of 3-amino-1-methyl-1,2-dicarba-closo-dodecaborane were prepared by means of resolution of the racemic mixture via acylation by (S)-naproxen chloride followed by separation and subsequent acid hydrolysis of each of the diastereoisomeric amides. Partial racemization of enantiomeric 3-aminocarboranes was observed during acid hydrolysis
\\\\Expert2\\nbo\\Tetrahedron Asymmetry\\2002, v.13, p.1833.pdf
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12.

Вид документа : Статья из журнала
Шифр издания : 54/K 46
Автор(ы) : Krasnov V. P., Levit G. L., Andreeva I.N., Grishakov A. N., Charushin V. N., Chupakhin O. N.
Заглавие : Kinetic resolution of (±)-2-methyl-1,2,3,4-tetrahydroquinoline and (±)-2-methylindoline [Electronic resource]
Место публикации : Mendeleev Communications. - 2002. - Vol. 12, № 1. - С. 27-28
Систем. требования: http://www.sciencedirect.com/science/article/pii/S0959943602705750
Примечания : 12.10.2011
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The acylation of racemic 2-methyl-1,2,3,4-tetrahydroquinoline and 2-methylindoline by (S)-naproxen acyl chloride resulted in their kinetic resolution with the predominant formation of (S,S)-diastereoisomeric amides (de 78–76%), recrystallisation of which followed by acid hydrolysis gave individual (S)-isomers of heterocyclic amines????
\\\\expert2\\nbo\\Mendeleev Communications\\2002, v.12, N 1. p.27.pdf
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13.

Вид документа : Статья из журнала
Шифр издания : 54/K 46
Автор(ы) : Krasnov V. P., Levit G. L., Bukrina I. M., Andreeva I.N., Sadretdinova L. Sh., Koroleva M. A., Kodess M. I., Charushin V. N., Chupakhin O. N.
Заглавие : Kinetic resolution of (±)-2,3-dihydro-3-methyl-4H-1,4-benzoxazine, (±)-2-methyl-1,2,3,4-tetrahydroquinoline and (±)-2-methylindoline using N-tosyl-(S)-prolyl chloride
Место публикации : Tetrahedron: Asymmetry . - 2003. - Vol. 14, № 14. - С. 1985-1988
Примечания : Bibliogr. : p. 1988 (6 ref.)
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Acylation of racemic 2,3-dihydro-3-methyl-4H-1,4-benzoxazine, 2-methyl-1,2,3,4-tetrahydroquinoline and 2-methylindoline with N-tosyl-(S)-prolyl chloride resulted in their kinetic resolution with the predominant formation of (R,S)-diastereoisomeric amides, des being 80, 66 and 38%, respectively. Recrystallisation of the amides followed by acid hydrolysis gave individual (R)-enantiomers of heterocyclic amines
\\\\Expert2\\nbo\\Tetrahedron Asymmetry\\2003, v.14, p.1985.pdf
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14.

Вид документа : Статья из журнала
Шифр издания : 54/C 52
Автор(ы) : Chizhov D. L., Roeschenthaler G.-V.
Заглавие : Reaction of trifluoromethylated beta-alkoxyenones with tris(trimethylsilyl) phosphite: A temperature influence on regioselectivity
Место публикации : Journal of Fluorine Chemistry. - 2006. - Vol. 127, № 2. - С. 235-239
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The interaction of tris(trimethylsilyl) phosphite (TMSO)3P and E-trifluoromethyl-alkoxyenones CF3C(O)CHCHOEt and CF3C(O)CHC(OMe)Me yielded mixtures of E-1,2- and Z-1,4-adducts, CF3C(OTMS)[P(O)(OTMS)2]CCH(OAlk)R 2 and CF3(OTMS)CCHCR(OAlk)[P(O)(OTMS)2] 3 where R and Alk = H and Me, or both Me. Conversion of these 1,2-adducts to 1,4-isomers was effected by increased temperature or by exposure to more tris(trimethylsilyl) phosphite. Acid hydrolysis of 2b (R and Alk = Me) gave ketophosphonic acid CF3C(OH)[P(O)(OH)2]CH2COMe in 88% yield, whereas hydrolysis of 2a (R = H and Alk = Et) with KOH in methanol gave CF3C(OH)[P(O)(OK)2]CHCHOEt in 37% yield. Acid hydrolysis of 3a (R = H and Alk = Et) and 3b (R and Alk = Me) gave phosphonic acid CF3C(OH)2CHCHP(O)(OH)2 in 82% yield and trifluoromethylated 1,2,5,4-oxaphosphol-3-en
\\\\Expert2\\nbo\\Journal of Fluorine Chemistry\\2006, v.127, p.235.pdf
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15.

Вид документа : Статья из журнала
Шифр издания : 54/N 10
Автор(ы) : Pestov A. V., Skorik Yu.A., Kogan G., Yatluk Yu. G.
Заглавие : N-alkylation of chitosan by beta-halopropionic acids in the presence of various acceptors
Место публикации : Journal of Applied Polymer Science . - 2008. - Vol. 108, № 1. - С. 119-127
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: N-carboxyethylation of chitosan by -halopropionic acids in the presence of various proton and halogen ion acceptors was investigated. It has been observed that carboxyethylation of chitosan in aqueous medium is accompanied by the by-processes of hydrolysis and dehydrohalogenation of the -halopropionic acids yielding -hydroxypropionic acid, bis(2-carbox-yethyl) ether, and acrylic acid. Degree of carboxyethyl substitution (DS) of chitosan and the relative rates of the by-processes varied significantly depending on the conditions used and nature of the proton or halogen ion acceptor. At carboxyethylation of chitosan with the alkaline -bromopropionates, the DS increased in the order Cs+ Rb- K+ sim; Na+ Li-.
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16.

Вид документа : Статья из сборника (однотомник)
Шифр издания : 54/C 52
Автор(ы) : Chizhov D. L., Charushin V. N., Roeschenthaler G.-V.
Заглавие : Convenient Rout to Regioisomeric Fluorinated Keto-Phosphonic Acids : доклад, тезисы доклада
Место публикации : 18th ISFC international Symposium on Fluorine Chemistry. Bremen, 30th Jul.-4 Aug. 2006 г. : Final Program. Abstracts. - Bremen, 2006. - С. 260
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
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17.

Вид документа : Статья из журнала
Шифр издания : 54/K 49
Автор(ы) : Kisil' S. P., Burgart Ya. V., Saloutin V. I.
Заглавие : New Fluoroaryl-containing beta,beta'-Dioxoesters in the Synthesis of Fluorobenzopyran-2(4)-ones [Electronic resource]
Место публикации : Russian Journal of Organic Chemistry (Translation of Zhurnal Organicheskoi Khimii). - 2001. - Vol. 37, № 10. - С. 1455-1462
Систем. требования: http://www.springerlink.com/content/kx6m35j2967226h7/fulltext.pdf
Примечания : 28.10.2011 г.
ББК : 54
Предметные 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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18.

Вид документа : Статья из сборника (однотомник)
Шифр издания : 54/А 50
Автор(ы) : Бердюгин Ю. А., Забелина О. Н., Первова М. Г., Кириченко В. Е., Ятлук Ю. Г.
Заглавие : Алкоголиз и гидролиз ПХБ
Параллельн. заглавия :Alcoholysis and hydrolysis PCB
Место публикации : Химия XXI век: новые технологии, новые продукты : тр. VIII Международной науч.-практ. конф., Кемерово, 10-12 мая 2005 г. - Кемерово, 2005. - С. 259-260: табл.
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
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19.

Вид документа : Статья из журнала
Шифр издания : 54/S 98
Автор(ы) : Saloutin V. I., Skryabina Z. E., Bazyl I. T., Chupakhin O. N.
Заглавие : Synthesis of 2(3)-ethoxycarbonyl-5,6,7,8-tetrafluorochromones [Electronic resource]
Место публикации : Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 1993. - Vol. 42, № 2. - С. 322-325
Систем. требования: http://www.springerlink.com/content/x67452m564465r80/fulltext.pdf
Примечания : 27.10.2011 г.
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The hitherto unknown ethyl pentafluorobenzoylpiruvate was prepared by condensing pentafluoroacetophenone with diethyl oxalate. Intramolecular cyclization of this ester or of its copper(II) chelate, as well as of ethyl 2-(ethoxymethylene)pentafluorobenzoylacetate affords 2- and 3-ethoxycarbonyl-5,6,7,8-tetrafluorochromones. Hydrolysis of the latter followed by decarboxylation gives 5,6,7,8-tetrafluorochromone
\\\\Expert2\\nbo\\Russian Chemical Bulletin\\1993, 42 (2), 322-325.pdf
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20.

Вид документа : Статья из журнала
Шифр издания : 54/P 80
Автор(ы) : Ostanina N.Yu., Dultseva L.D., Suvorov A. L., Chupakhin O. N.
Заглавие : Polymers Based on Epoxy Resins and Functional Derivatives of Polychlorobiphenyls [Electronic resource]
Место публикации : Russian Journal of Applied Chemistry. - 2002. - Vol. 75, № 5. - С. 814-817
Систем. требования: http://www.springerlink.com/content/t78n622000534516/fulltext.pdf
Примечания : 19.10.2011
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: A new way to utilize polychlorobiphenyls was suggested: transformation of Sovol base hydrolysis products into glycidyl ethers and titanates. The resulting products were tested as components of epoxy compounds which are subsequently cured to obtain three-dimensional polymer networks
\\\\Expert2\\nbo\\Russian Journal of Applied Chemistry\\2002, v. 75, N. 5, p.814.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

Сиглы библиотек институтов и НЦ УрО РАН

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