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Automated Chemical Oligosaccharide Synthesis: Novel Approach to Traditional Challenges

Chemical reviews, 2018-09, Vol.118 (17), p.8105-8150

2018

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Koenigs–Knorr Glycosylation Reaction Catalyzed by Trimethylsilyl Trifluoromethanesulfonate

Chemistry : a European journal, 2019-01, Vol.25 (6), p.1461-1465

2019

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The 4K reaction

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

2024

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Development of an Arming Participating Group for Stereoselective Glycosylation and Chemoselective Oligosaccharide Synthesis

Angewandte Chemie (International ed.), 2005-11, Vol.44 (43), p.7123-7126

2005

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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

Chemistry : a European journal, 2015-04, Vol.21 (17), p.6572-6581

2015

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A Highly Efficient Glycosidation of Glycosyl Chlorides by Using Cooperative Silver(I) Oxide–Triflic Acid Catalysis

Chemistry : a European journal, 2020-06, Vol.26 (36), p.8053-8063

2020

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Chemical Synthesis of Human Milk Oligosaccharides: para‐Lacto‐N‐hexaose and para‐Lacto‐N‐neohexaose

Chemistry : a European journal, 2023-11, Vol.29 (64), p.e202302288-n/a

2023

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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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Identification of a Simple Chemical Structure Associated with Protective Human Antibodies against Multiple Pneumococcal Serogroups

Infection and Immunity, 2009-08, Vol.77 (8), p.3374-3379

2009

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S-Thiazolinyl (STaz) Glycosides as Versatile Building Blocks for Convergent Selective, Chemoselective, and Orthogonal Oligosaccharide Synthesis

Chemistry : a European journal, 2006-08, Vol.12 (25), p.6630-6646

2006

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Carbohydrate Experiments in the Organic Laboratory: A Robust Synthesis and Modification of Thioglycosides

Journal of chemical education, 2019-10, Vol.96 (10), p.2322-2325

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

Angewandte Chemie (International ed.), 2011-04, Vol.50 (18), p.4197-4201

International ed. in English, 2011

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Extending the S-benzimidazolyl (SBiz) platform: N-alkylated SBiz glycosyl donors with the universal activation profile

Pure and applied chemistry, 2017-09, Vol.89 (9), p.1321-1331

2017

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Electrochemical impedance spectroscopy study of Concanavalin A binding to self-assembled monolayers of mannosides on gold wire electrodes

Journal of electroanalytical chemistry (Lausanne, Switzerland), 2016-11, Vol.780, p.311-320

2016

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Electrochemical impedance spectroscopy study of carbohydrate-terminated alkanethiol monolayers on nanoporous gold: Implications for pore wetting

Journal of electroanalytical chemistry (Lausanne, Switzerland), 2016-12, Vol.782, p.174-181

2016

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From Stereocontrolled Glycosylation to Expeditious Oligosaccharide Synthesis

Trends in Glycoscience and Glycotechnology, 2013, Vol.25(141), pp.13-42

2013

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Potent, Versatile, and Stable: Thiazolyl Thioglycosides as Glycosyl Donors

Angewandte Chemie (International ed.), 2004-06, Vol.43 (23), p.3069-3072

2004

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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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Synthesis, characterization and reactivity of carbohydrate platinum(IV) complexes with thioglycoside ligands

Dalton transactions : an international journal of inorganic chemistry, 2010-01, Vol.39 (27), p.6327-6338

2010

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Synthesis, Conjugation, and Immunological Evaluation of the Serogroup 6 Pneumococcal Oligosaccharides

Chembiochem : a European journal of chemical biology, 2009-12, Vol.10 (18), p.2893-2899

2009

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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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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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Nickel(II) Chloride-Mediated Regioselective Benzylation and Benzoylation of Diequatorial Vicinal Diols

Synlett, 2004-10, Vol.2004 (12), p.2191-2193

2004

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立体選択的グリコシル化から迅速オリゴ糖合成まで

Trends in Glycoscience and Glycotechnology, 2013, Vol.25(141), pp.13-42

2013

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Automated Chemical Oligosaccharide Synthesis: Novel Approach to Traditional Challenges

Koenigs–Knorr Glycosylation Reaction Catalyzed by Trimethylsilyl Trifluoromethanesulfonate

The 4K reaction

Development of an Arming Participating Group for Stereoselective Glycosylation and Chemoselective Oligosaccharide Synthesis

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

A Highly Efficient Glycosidation of Glycosyl Chlorides by Using Cooperative Silver(I) Oxide–Triflic Acid Catalysis

Chemical Synthesis of Human Milk Oligosaccharides: para‐Lacto‐N‐hexaose and para‐Lacto‐N‐neohexaose

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

Identification of a Simple Chemical Structure Associated with Protective Human Antibodies against Multiple Pneumococcal Serogroups

S-Thiazolinyl (STaz) Glycosides as Versatile Building Blocks for Convergent Selective, Chemoselective, and Orthogonal Oligosaccharide Synthesis

Carbohydrate Experiments in the Organic Laboratory: A Robust Synthesis and Modification of Thioglycosides

Synthesis of oligosaccharide fragments of capsular polysaccharide Staphylococcus aureus type 8

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

Extending the S-benzimidazolyl (SBiz) platform: N-alkylated SBiz glycosyl donors with the universal activation profile

Electrochemical impedance spectroscopy study of Concanavalin A binding to self-assembled monolayers of mannosides on gold wire electrodes

Electrochemical impedance spectroscopy study of carbohydrate-terminated alkanethiol monolayers on nanoporous gold: Implications for pore wetting

From Stereocontrolled Glycosylation to Expeditious Oligosaccharide Synthesis

Potent, Versatile, and Stable: Thiazolyl Thioglycosides as Glycosyl Donors

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

Synthesis, characterization and reactivity of carbohydrate platinum(IV) complexes with thioglycoside ligands

Synthesis, Conjugation, and Immunological Evaluation of the Serogroup 6 Pneumococcal Oligosaccharides

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”.)

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

Nickel(II) Chloride-Mediated Regioselective Benzylation and Benzoylation of Diequatorial Vicinal Diols

立体選択的グリコシル化から迅速オリゴ糖合成まで

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