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Handbook of chemical glycosylation: advances in stereoselectivity and therapeutic relevance.

Demchenko, Alexei V

1, 2008

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Expeditious oligosaccharide synthesis via selective, semi-orthogonal, and orthogonal activation

Carbohydrate research, 2011-09, Vol.346 (12), p.1371-1388

2011

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The 4K reaction

Carbohydrate research, 2024-04, Vol.538, p.109102-109102, Article 109102

2024

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Frontispiece: Transition‐Metal‐Mediated Glycosylation with Thioglycosides

Chemistry : a European journal, 2022-03, Vol.28 (14), p.n/a

2022

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Expanding the scope of stereoselective α-galactosylation using glycosyl chlorides

Bioorganic & medicinal chemistry, 2022-11, Vol.73, p.117031-117031, Article 117031

2022

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Chemical synthesis of human milk oligosaccharides: lacto-N-neohexaose (Galβ1 → 4GlcNAcβ1→) 2 3,6Galβ1 → 4Glc

Organic & biomolecular chemistry, 2020-03, Vol.18 (9), p.1747-1753

2020

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N‐Alkylated Analogues of Indolylthio Glycosides as Glycosyl Donors with Enhanced Activation Profile

European journal of organic chemistry, 2022-05, Vol.2022 (18), p.n/a

2022

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Chemical Synthesis of Human Milk Oligosaccharides: Lacto‑N‑hexaose Galβ1→3GlcNAcβ1→3 [Galβ1→4GlcNAcβ1→6] Galβ1→4Glc

Journal of organic chemistry, 2019-12, Vol.84 (24), p.16192-16198

2019

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Synthesis of oligosaccharide fragments of capsular polysaccharide Staphylococcus aureus type 8

Journal of carbohydrate chemistry, 2020-09, Vol.39 (7), p.301-333

2020

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Development of a Simple and Effective Lipid‑A Antagonist Based on Computational Prediction

ACS infectious diseases, 2022-06, Vol.8 (6), p.1171-1178

2022

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Carbohydrates: Synthesis, Mechanisms, and Stereoelectronic Effects

Journal of the American Chemical Society, 2010-11, Vol.132 (45), p.16297-16297

Demchenko, Alexei V

2010

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Chapter 5 Oligosaccharide Synthesis: From Conventional Methods to Modern Expeditious Strategies

Advances in Carbohydrate Chemistry and Biochemistry, 2009, Vol.62, p.161-250

2009

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Front Cover: Defining the Scope of the Acid‐Catalyzed Glycosidation of Glycosyl Bromides (Chem. Eur. J. 5/2020)

Chemistry : a European journal, 2020-01, Vol.26 (5), p.959-959

2020

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Synthesis of carbohydrate building blocks regioselective uniform protection/deprotection strategies

Organic & biomolecular chemistry, 2019-05, Vol.17 (2), p.4934-495

2019

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S‐Benzimidazolyl Glycosides as a Platform for Oligosaccharide Synthesis by an Active–Latent Strategy

Angewandte Chemie, 2011-04, Vol.123 (18), p.4283-4287

2011

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Hydrogen Bond Mediated Aglycone Delivery: Synthesis of Linear and Branched α-Glucans

Angewandte Chemie, 2014-09, Vol.126 (39), p.10621-10624

2014

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Iron(iii) chloride-catalyzed activation of glycosyl chloridesElectronic supplementary information (ESI) available: Experimental details and characterization data for all new compounds. See DOI: 10.1039/c8ob02413h

2018-12

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Chemical synthesis of human milk oligosaccharides: lacto--neohexaose (Galβ1 → 4GlcNAcβ1→) 3,6Galβ1 → 4Glc

Organic & biomolecular chemistry, 2020-03, Vol.18 (9), p.1747-1753

2020

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capsular polysaccharides: a structural and synthetic perspective

Organic & biomolecular chemistry, 2020-02, Vol.18 (5), p.783-798

2020

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Hydrogen-Bond-Mediated Aglycone Delivery (HAD): A Highly Stereoselective Synthesis of 1,2-cis [alpha]-D-Glucosides from Common Glycosyl Donors in the Presence of Bromine

Chemistry : a European journal, 2015-04, Vol.21 (17), p.6572

2015

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Picoloyl protecting group in synthesis: focus on a highly chemoselective catalytic removal (Dedicated to the memory of Bert Fraser-Reid (1934–2020) who was among the first to recognize the effect of protecting groups in carbohydrate chemistry “Protecting groups do more than protect”.)

Organic & biomolecular chemistry, 2020-01, Vol.18 (25), p.4863-4871

2020

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Hydrogen Bond Mediated Aglycone Delivery: Synthesis of Linear and Branched [alpha]-Glucans

Angewandte Chemie (International ed.), 2014-09, Vol.53 (39), p.10453

International ed. in English, 2014

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General Aspects of the Glycosidic Bond Formation

Handbook of Chemical Glycosylation, 2008, p.1-27

Demchenko, Alexei V

2008

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Stereocontrolled 1,2-cisglycosylation as the driving force of progress in synthetic carbohydrate chemistry

Chemical science (Cambridge), 2015-04, Vol.6 (5), p.2687-2704

2015

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Glycosyl nitrates in synthesis: streamlined access to glucopyranose building blocks differentiated at C-2Electronic supplementary information (ESI) available: 1H and 13C NMR spectra for all new compounds have been supplied as the ESI. Table of calculated and observed X-ray structure factors for compounds 10, 13, and 14. CCDC 1814198-1814200. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c8ob00477c

2018-05

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Handbook of chemical glycosylation: advances in stereoselectivity and therapeutic relevance.

Expeditious oligosaccharide synthesis via selective, semi-orthogonal, and orthogonal activation

The 4K reaction

Frontispiece: Transition‐Metal‐Mediated Glycosylation with Thioglycosides

Expanding the scope of stereoselective α-galactosylation using glycosyl chlorides

Chemical synthesis of human milk oligosaccharides: lacto-N-neohexaose (Galβ1 → 4GlcNAcβ1→) 2 3,6Galβ1 → 4Glc

N‐Alkylated Analogues of Indolylthio Glycosides as Glycosyl Donors with Enhanced Activation Profile

Chemical Synthesis of Human Milk Oligosaccharides: Lacto‑N‑hexaose Galβ1→3GlcNAcβ1→3 [Galβ1→4GlcNAcβ1→6] Galβ1→4Glc

Synthesis of oligosaccharide fragments of capsular polysaccharide Staphylococcus aureus type 8

Development of a Simple and Effective Lipid‑A Antagonist Based on Computational Prediction

Carbohydrates: Synthesis, Mechanisms, and Stereoelectronic Effects

Chapter 5 Oligosaccharide Synthesis: From Conventional Methods to Modern Expeditious Strategies

Front Cover: Defining the Scope of the Acid‐Catalyzed Glycosidation of Glycosyl Bromides (Chem. Eur. J. 5/2020)

Synthesis of carbohydrate building blocks regioselective uniform protection/deprotection strategies

S‐Benzimidazolyl Glycosides as a Platform for Oligosaccharide Synthesis by an Active–Latent Strategy

Hydrogen Bond Mediated Aglycone Delivery: Synthesis of Linear and Branched α-Glucans

Iron(iii) chloride-catalyzed activation of glycosyl chloridesElectronic supplementary information (ESI) available: Experimental details and characterization data for all new compounds. See DOI: 10.1039/c8ob02413h

Chemical synthesis of human milk oligosaccharides: lacto--neohexaose (Galβ1 → 4GlcNAcβ1→) 3,6Galβ1 → 4Glc

capsular polysaccharides: a structural and synthetic perspective

Hydrogen-Bond-Mediated Aglycone Delivery (HAD): A Highly Stereoselective Synthesis of 1,2-cis [alpha]-D-Glucosides from Common Glycosyl Donors in the Presence of Bromine

Picoloyl protecting group in synthesis: focus on a highly chemoselective catalytic removal (Dedicated to the memory of Bert Fraser-Reid (1934–2020) who was among the first to recognize the effect of protecting groups in carbohydrate chemistry “Protecting groups do more than protect”.)

Hydrogen Bond Mediated Aglycone Delivery: Synthesis of Linear and Branched [alpha]-Glucans

General Aspects of the Glycosidic Bond Formation

Stereocontrolled 1,2-cisglycosylation as the driving force of progress in synthetic carbohydrate chemistry

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