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Phase-Transfer Catalyzed Microfluidic Glycosylation: A Small Change in Concentration Results in a Dramatic Increase in Stereoselectivity

Catalysts, 2023-02, Vol.13 (2), p.313

2023

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Mixer Design and Flow Rate as Critical Variables in Flow Chemistry Affecting the Outcome of a Chemical Reaction: A Review

Inventions (Basel), 2023-10, Vol.8 (5), p.128

2023

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Editorial: Chemical reactivity and solution structure

Frontiers in chemistry, 2023-09, Vol.11, p.1293697-1293697

2023

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A Ring Contraction of 2,3-Di‑O‑Silylated Thiopyranosides To Give Thiofuranosides under Mildly Acidic Conditions

Organic letters, 2018-10, Vol.20 (19), p.6051-6054

2018

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Comparison of glycosyl donors: a supramer approach

Beilstein journal of organic chemistry, 2024, Vol.20 (1), p.181-192

2024

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Concentration Dependence of Glycosylation Outcome: A Clue to Reproducibility and Understanding the Reasons Behind

European journal of organic chemistry, 2012-04, Vol.2012 (10), p.1926-1934

2012

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Preparation and in vivo evaluation of glyco-gold nanoparticles carrying synthetic mycobacterial hexaarabinofuranoside

Beilstein journal of nanotechnology, 2020, Vol.11 (1), p.480-493

2020

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Synthesis of branched arabinofuranose pentasaccharide fragment of mycobacterial arabinans as 2-azidoethyl glycoside

Carbohydrate research, 2012-08, Vol.357, p.62-67

2012

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Synthesis of sialyl halides with various acyl protective groups

Carbohydrate research, 2024-02, Vol.536, p.109033-109033, Article 109033

2024

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Synthesis and study of the glycosyl-donor properties of 2-(2,2,2-trichloroethoxy)-(3,4,6-tri-O-acetyl-1,2-dideoxy-α-d-galactopyrano)-[2,1-d]-2-oxazoline

Carbohydrate research, 2024-02, Vol.536, p.109040-109040, Article 109040

2024

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Exhaustive Conformational Search for Sialyl Cation Reveals Possibility of Remote Participation of Acyl Groups

Chemphyschem, 2022-02, Vol.23 (3), p.e202100788-n/a

2022

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Five Triisopropylsilyl Substituents in Ara‐β‐(1→2)‐Ara Disaccharide Glycosyl Donor Make Unselective Glycosylation Reaction Stereoselective

European journal of organic chemistry, 2022-12, Vol.2022 (46), p.n/a

2022

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Unusual triflic acid-promoted oligomerization of arabinofuranosides during glycosylation

Carbohydrate research, 2024-06, Vol.540, p.109141-109141, Article 109141

2024

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TIPS group-assisted isomerization of benzyl protected d-manno- and d-glucopyranose to d-fructofuranose derivatives

Carbohydrate research, 2023-12, Vol.534, p.108942-108942, Article 108942

2023

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Mild and General Protocol for Selective Deacetylation of Acetyl/Benzoyl-Protected Carbohydrates

Journal of organic chemistry, 2024-07, Vol.89 (14), p.10021-10026

2024

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Black Swan in Phase Transfer Catalysis: Influence of Mixing Mode on the Stereoselectivity of Glycosylation

European journal of organic chemistry, 2022-04, Vol.2022 (14), p.n/a

2022

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Pectin–glycerol gel beads: Preparation, characterization and swelling behaviour

Carbohydrate polymers, 2020-06, Vol.238, p.116166-116166, Article 116166

2020

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Stereocontrolling Effect of a Single Triisopropylsilyl Group in 1,2‐cis‐Glucosylation

European journal of organic chemistry, 2022-10, Vol.2022 (39), p.n/a

2022

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New methods for the synthesis of 2-(2,2,2-trichloroethoxy)-(3,4,6-tri-O-acetyl-1,2-dideoxy-α-D-glucopyrano)-[2,1-d]-2-oxazoline and its use for stereo-, chemo- and regioselective glycosylation

Carbohydrate research, 2022-10, Vol.520, p.108633-108633, Article 108633

2022

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Unusual Outcome of Glycosylation: Hydrogen‐Bond Mediated Control of Stereoselectivity by N‐Trifluoroacetyl Group?

European journal of organic chemistry, 2020-07, Vol.2020 (27), p.4146-4160

2020

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Rapid synthesis of linear homologous oligoarabinofuranosides related to mycobacterial lipoarabinomannan and a neoglycoconjugate thereof

Carbohydrate research, 2016-08, Vol.431, p.25-32

2016

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Janus glycosides of next generation: Synthesis of 4-(3-chloropropoxy)phenyl and 4-(3-azidopropoxy)phenyl glycosides

Carbohydrate research, 2019-01, Vol.471, p.95-104

2019

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Application of a Janus aglycon with dual function in benzyl-free synthesis of spacer-armed oligosaccharide fragments of polysaccharides from rhizobacterium Azospirillum brasilense sp7

Carbohydrate research, 2018-07, Vol.464, p.28-43

2018

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Light Scattering in Non-aqueous Solutions of Low-Molecular-Mass Compounds: Application for Supramer Analysis of Reaction Solutions

Journal of solution chemistry, 2020-05, Vol.49 (5), p.629-644

2020

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The use of the novel glycosyl acceptor and supramer analysis in the synthesis of sialyl-α(2–3)-galactose building block

Carbohydrate research, 2018-12, Vol.470, p.27-35

2018

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Phase-Transfer Catalyzed Microfluidic Glycosylation: A Small Change in Concentration Results in a Dramatic Increase in Stereoselectivity

Mixer Design and Flow Rate as Critical Variables in Flow Chemistry Affecting the Outcome of a Chemical Reaction: A Review

Editorial: Chemical reactivity and solution structure

A Ring Contraction of 2,3-Di‑O‑Silylated Thiopyranosides To Give Thiofuranosides under Mildly Acidic Conditions

Comparison of glycosyl donors: a supramer approach

Concentration Dependence of Glycosylation Outcome: A Clue to Reproducibility and Understanding the Reasons Behind

Preparation and in vivo evaluation of glyco-gold nanoparticles carrying synthetic mycobacterial hexaarabinofuranoside

Synthesis of branched arabinofuranose pentasaccharide fragment of mycobacterial arabinans as 2-azidoethyl glycoside

Synthesis of sialyl halides with various acyl protective groups

Synthesis and study of the glycosyl-donor properties of 2-(2,2,2-trichloroethoxy)-(3,4,6-tri-O-acetyl-1,2-dideoxy-α-d-galactopyrano)-[2,1-d]-2-oxazoline

Exhaustive Conformational Search for Sialyl Cation Reveals Possibility of Remote Participation of Acyl Groups

Five Triisopropylsilyl Substituents in Ara‐β‐(1→2)‐Ara Disaccharide Glycosyl Donor Make Unselective Glycosylation Reaction Stereoselective

Unusual triflic acid-promoted oligomerization of arabinofuranosides during glycosylation

TIPS group-assisted isomerization of benzyl protected d-manno- and d-glucopyranose to d-fructofuranose derivatives

Mild and General Protocol for Selective Deacetylation of Acetyl/Benzoyl-Protected Carbohydrates

Black Swan in Phase Transfer Catalysis: Influence of Mixing Mode on the Stereoselectivity of Glycosylation

Pectin–glycerol gel beads: Preparation, characterization and swelling behaviour

Stereocontrolling Effect of a Single Triisopropylsilyl Group in 1,2‐cis‐Glucosylation

New methods for the synthesis of 2-(2,2,2-trichloroethoxy)-(3,4,6-tri-O-acetyl-1,2-dideoxy-α-D-glucopyrano)-[2,1-d]-2-oxazoline and its use for stereo-, chemo- and regioselective glycosylation

Unusual Outcome of Glycosylation: Hydrogen‐Bond Mediated Control of Stereoselectivity by N‐Trifluoroacetyl Group?

Rapid synthesis of linear homologous oligoarabinofuranosides related to mycobacterial lipoarabinomannan and a neoglycoconjugate thereof

Janus glycosides of next generation: Synthesis of 4-(3-chloropropoxy)phenyl and 4-(3-azidopropoxy)phenyl glycosides

Application of a Janus aglycon with dual function in benzyl-free synthesis of spacer-armed oligosaccharide fragments of polysaccharides from rhizobacterium Azospirillum brasilense sp7

Light Scattering in Non-aqueous Solutions of Low-Molecular-Mass Compounds: Application for Supramer Analysis of Reaction Solutions

The use of the novel glycosyl acceptor and supramer analysis in the synthesis of sialyl-α(2–3)-galactose building block

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