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Публикации в базе данных Math-Net.Ru
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3-Амино-3-дезокси- и 4-амино-4-дезоксигексозы в синтезе природных углеводных структур и их аналогов
Усп. хим., 90:2 (2021), 171–198
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New hybrid furoxan structures with antiaggregant activity
Mendeleev Commun., 28:6 (2018), 595–597
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Antiaggregant activity of water-soluble furoxans
Mendeleev Commun., 28:1 (2018), 49–51
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Organic and hybrid systems: from science to practice
Mendeleev Commun., 27:5 (2017), 425–438
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Синтез олигосахаридов, родственных полисахаридам клеточной стенки грибов Candida и Aspergillus
Усп. хим., 86:11 (2017), 1073–1126
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New insight into the antiaggregant activity of furoxans
Mendeleev Commun., 26:6 (2016), 513–515
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Pyranoside-into-furanoside rearrangement of D-glucuronopyranoside derivatives
Mendeleev Commun., 26:6 (2016), 483–484
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Challenges in the development of organic and hybrid molecular systems
Mendeleev Commun., 26:5 (2016), 365–374
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Near IR spectroscopy of the solutions of a bacteriochlorin derivative as a quantitative method for the quality assurance of liquid products
Mendeleev Commun., 26:3 (2016), 261–263
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Sensitivity of magnetic resonance imaging based on the detection of 19F NMR signals
Mendeleev Commun., 26:1 (2016), 24–25
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High-resolution mass spectra of biotinylated, HEG-spacered molecular probes with oligosaccharide fragments of the capsular polysaccharides from Streptococcus pneumoniae
Mendeleev Commun., 25:6 (2015), 457–459
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Computational study of the possible formation of the ternary complex between thrombin, antithrombin III and fucosylated chondroitin sulfates
Mendeleev Commun., 25:6 (2015), 420–421
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Organic and hybrid molecular systems
Mendeleev Commun., 25:2 (2015), 75–82
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Paзpaбoткa пoдxoдoв к coздaнию yглeвoднoй кoнъюгиpoвaннoй вaкцины тpeтьeгo пoкoлeния пpoтив Streptococcus pneumoniae: пoиcк oптимaльныx oлигocaxapидныx лигaндoв
Усп. хим., 84:11 (2015), 1100–1113
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Preparative synthesis of selectively substituted 1,6-anhydro-α-D-galactofuranose derivatives
Mendeleev Commun., 24:6 (2014), 336–337
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Гликоконъюгаты порфиринов с углеводами: методы синтеза и биологическая активность
Усп. хим., 83:6 (2014), 523–554
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Применение современных методов спектроскопии ЯМР для конформационного анализа олиго- и полисахаридов
Усп. хим., 78:8 (2009), 776–795
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Homogeneous azidophenylselenylation of glucals
Mendeleev Commun., 18:5 (2008), 241–243
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Modeling of polysaccharides with oligosaccharides: how large should the model be?
Mendeleev Commun., 17:2 (2007), 57–62
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Effect of the nature of protecting group at O-4 on stereoselectivity of glycosylation by 4-O-substituted 2,3-di-O-benzylfucosyl bromides
Mendeleev Commun., 9:3 (1999), 114–116
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Synthesis of neoglycoconjugate dendrimers
Mendeleev Commun., 9:2 (1999), 47–50
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Synthesis of spacer-armed glycosides using azidophenylselenylation of allyl glycosides
Mendeleev Commun., 8:1 (1998), 9–12
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