Works matching AU Demchenko, Alexei V.
Results: 43
Front Cover: HPLC‐Based Automated Synthesis and Purification of Carbohydrates (Chem. Eur. J. 43/2024).
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- Chemistry - A European Journal, 2024, v. 30, n. 43, p. 1, doi. 10.1002/chem.202402504
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HPLC‐Based Automated Synthesis and Purification of Carbohydrates.
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- Chemistry - A European Journal, 2024, v. 30, n. 43, p. 1, doi. 10.1002/chem.202401214
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Chemical Synthesis of Human Milk Oligosaccharides: para‐Lacto‐N‐hexaose and para‐Lacto‐N‐neohexaose.
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- Chemistry - A European Journal, 2023, v. 29, n. 64, p. 1, doi. 10.1002/chem.202302288
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Cooperatively Catalyzed Activation of Thioglycosides That Bypasses Intermediacy of Glycosyl Halides.
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- Chemistry - A European Journal, 2023, v. 29, n. 43, p. 1, doi. 10.1002/chem.202300873
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HPLC‐Based Automated Synthesis of Glycans in Solution.
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- Chemistry - A European Journal, 2022, v. 28, n. 39, p. 1, doi. 10.1002/chem.202201180
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Synthesis of oligosaccharide fragments of capsular polysaccharide Staphylococcus aureus type 8.
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- Journal of Carbohydrate Chemistry, 2020, v. 39, n. 7, p. 301, doi. 10.1080/07328303.2020.1821042
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Immobilization of glycans on solid surfaces for application in glycomics.
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- Journal of Carbohydrate Chemistry, 2018, v. 37, n. 4, p. 225, doi. 10.1080/07328303.2018.1462372
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Hydrolysis of Glycosyl Thioimidates by Glycoside Hydrolase Requires Remote Activation for Efficient Activity.
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- Catalysts (2073-4344), 2019, v. 9, n. 10, p. 826, doi. 10.3390/catal9100826
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Extending the S-benzimidazolyl (SBiz) platform: N-alkylated SBiz glycosyl donors with the universal activation profile.
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- Pure & Applied Chemistry, 2017, v. 89, n. 9, p. 1321, doi. 10.1515/pac-2017-0112
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S-Benzimidazolyl Glycosides as a Platform for Oligosaccharide Synthesis by an Active-Latent Strategy.
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- Angewandte Chemie International Edition, 2011, v. 50, n. 18, p. 4197, doi. 10.1002/anie.201007212
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Synthesis, Conjugation, and Immunological Evaluation of the Serogroup 6 Pneumococcal Oligosaccharides.
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- ChemBioChem, 2009, v. 10, n. 18, p. 2893, doi. 10.1002/cbic.200900587
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Nanoporous Gold Monolith for High Loading of Unmodified Doxorubicin and Sustained Co-Release of Doxorubicin-Rapamycin.
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- Nanomaterials (2079-4991), 2021, v. 11, n. 1, p. 208, doi. 10.3390/nano11010208
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Preparation, Modification, Characterization, and Biosensing Application of Nanoporous Gold Using Electrochemical Techniques.
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- Nanomaterials (2079-4991), 2018, v. 8, n. 3, p. 171, doi. 10.3390/nano8030171
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N‐Alkylated Analogues of Indolylthio Glycosides as Glycosyl Donors with Enhanced Activation Profile.
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- European Journal of Organic Chemistry, 2022, v. 2022, n. 18, p. 1, doi. 10.1002/ejoc.202200300
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Direct Glycosidation of 2‐Azido‐2‐deoxyglycosyl Nitrates.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 37, p. 6413, doi. 10.1002/ejoc.201900748
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Investigation of Glycosyl Nitrates as Building Blocks for Chemical Glycosylation.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 47, p. 6699, doi. 10.1002/ejoc.201801272
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A Novel Direct Glycosylation Approach for the Synthesis of Dimers of N-Acetylneuraminic Acid.
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- Chemistry - A European Journal, 1999, v. 5, n. 4, p. 1278, doi. 10.1002/(sici)1521-3765(19990401)5:4<1278::aid-chem1278>3.3.co;2-c
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Thermophysical properties in medium temperature range of several thio and dithiocarbamates.
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- Journal of Thermal Analysis & Calorimetry, 2008, v. 91, n. 2, p. 471, doi. 10.1007/s10973-007-8345-8
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Ferric Chloride Promoted Glycosidation of Alkyl Thioglycosides.
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- Molecules, 2024, v. 29, n. 20, p. 4845, doi. 10.3390/molecules29204845
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Activation of Thioglycosides with Copper(II) Bromide.
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- Molecules, 2022, v. 27, n. 21, p. 7354, doi. 10.3390/molecules27217354
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Applications of Nanoporous Gold in Therapy, Drug Delivery, and Diagnostics.
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- Metals (2075-4701), 2023, v. 13, n. 1, p. 78, doi. 10.3390/met13010078
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Frontispiece: Transition‐Metal‐Mediated Glycosylation with Thioglycosides.
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- Chemistry - A European Journal, 2022, v. 28, n. 14, p. 1, doi. 10.1002/chem.202281461
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Transition‐Metal‐Mediated Glycosylation with Thioglycosides.
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- Chemistry - A European Journal, 2022, v. 28, n. 14, p. 1, doi. 10.1002/chem.202103747
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A Streamlined Regenerative Glycosylation Reaction: Direct, Acid‐Free Activation of Thioglycosides.
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- Chemistry - A European Journal, 2021, v. 27, n. 1, p. 354, doi. 10.1002/chem.202003479
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A Highly Efficient Glycosidation of Glycosyl Chlorides by Using Cooperative Silver(I) Oxide–Triflic Acid Catalysis.
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- Chemistry - A European Journal, 2020, v. 26, n. 36, p. 8053, doi. 10.1002/chem.201905576
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Synthesis of β‐Glucosides with 3‐O‐Picoloyl‐Protected Glycosyl Donors in the Presence of Excess Triflic Acid: Defining the Scope.
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- Chemistry - A European Journal, 2020, v. 26, n. 13, p. 2938, doi. 10.1002/chem.201905278
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Synthesis of β‐Glucosides with 3‐O‐Picoloyl‐Protected Glycosyl Donors in the Presence of Excess Triflic Acid: A Mechanistic Study.
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- Chemistry - A European Journal, 2020, v. 26, n. 13, p. 2927, doi. 10.1002/chem.201905277
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Defining the Scope of the Acid‐Catalyzed Glycosidation of Glycosyl Bromides.
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- Chemistry - A European Journal, 2020, v. 26, n. 5, p. 963, doi. 10.1002/chem.201905187
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Front Cover: Defining the Scope of the Acid‐Catalyzed Glycosidation of Glycosyl Bromides (Chem. Eur. J. 5/2020).
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- Chemistry - A European Journal, 2020, v. 26, n. 5, p. 959, doi. 10.1002/chem.201905186
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Defining the Scope of the Acid‐Catalyzed Glycosidation of Glycosyl Bromides.
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- Chemistry - A European Journal, 2020, v. 26, n. 5, p. 1042, doi. 10.1002/chem.201904185
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Bromine‐Promoted Glycosidation of Conformationally Superarmed Thioglycosides.
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- Chemistry - A European Journal, 2019, v. 25, n. 51, p. 11831, doi. 10.1002/chem.201901969
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Koenigs–Knorr Glycosylation Reaction Catalyzed by Trimethylsilyl Trifluoromethanesulfonate.
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- Chemistry - A European Journal, 2019, v. 25, n. 6, p. 1461, doi. 10.1002/chem.201805527
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S-Benzimidazolyl Glycosides as a Platform for Oligosaccharide Synthesis by an Active-Latent Strategy.
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- Angewandte Chemie, 2011, v. 123, n. 18, p. 4283, doi. 10.1002/ange.201007212
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Development of an Arming Participating Group for Stereoselective Glycosylation and Chemoselective Oligosaccharide Synthesis.
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- Angewandte Chemie, 2005, v. 117, n. 43, p. 7285, doi. 10.1002/ange.200502694
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Potent, Versatile, and Stable: Thiazolyl Thioglycosides as Glycosyl DonorsThis work was supported by the University of Missouri Research Board and “The Foundation BLANCEFLOR Boncompagni-Ludovisi, née Bildt”.
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- Angewandte Chemie, 2004, v. 116, n. 23, p. 3131, doi. 10.1002/ange.200454047
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Recent Advances in Stereocontrolled Mannosylation: Focus on Glycans Comprising Acidic and/or Amino Sugars.
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- Chemical Record, 2021, v. 21, n. 11, p. 3278, doi. 10.1002/tcr.202100201
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Hydrogen-Bond-Mediated Aglycone Delivery (HAD): A Highly Stereoselective Synthesis of 1,2- cis α- D-Glucosides from Common Glycosyl Donors in the Presence of Bromine.
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- Chemistry - A European Journal, 2015, v. 21, n. 17, p. 6572, doi. 10.1002/chem.201406589
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Hydrogen Bond Mediated Aglycone Delivery: Synthesis of Linear and Branched α-Glucans.
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- Angewandte Chemie, 2014, v. 126, n. 39, p. 10621, doi. 10.1002/ange.201405084
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Development of an Arming Participating Group for Stereoselective Glycosylation and Chemoselective Oligosaccharide SynthesisThe authors thank the University of Missouri–St. Louis and the ACS PRF 42397-G1 for financial support of this research; the NSF for grants to purchase an NMR spectrometer (CHE-9974801) and the mass spectrometer (CHE-9708640) used in this work, Dr. R. S. Luo for assistance with 500 MHz 2D NMR experiments, and Dr. R. E. K. Winter and Mr. J. Kramer for HRMS determinations.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 43, p. 7123, doi. 10.1002/anie.200502694
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Potent, Versatile, and Stable: Thiazolyl Thioglycosides as Glycosyl Donors.
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- Angewandte Chemie International Edition, 2004, v. 43, n. 23, p. 3069, doi. 10.1002/anie.200454047
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S-Thiazolinyl (STaz) Glycosides as Versatile Building Blocks for Convergent Selective, Chemoselective, and Orthogonal Oligosaccharide Synthesis.
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- Chemistry - A European Journal, 2006, v. 12, n. 25, p. 6630, doi. 10.1002/chem.200600262
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Remote Participation-Assisted Synthesis of β-Mannosides.
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- European Journal of Organic Chemistry, 2005, v. 2005, n. 4, p. 706, doi. 10.1002/ejoc.200400616
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Hydrogen Bond Mediated Aglycone Delivery: Synthesis of Linear and Branched α-Glucans.
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- Angewandte Chemie International Edition, 2014, v. 53, n. 39, p. 10453, doi. 10.1002/anie.201405084
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