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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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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 photoactivable oligosaccharide derivatives from 1,2-cyclic carbamate building blocks and study of their interaction with carbohydrate-binding proteins

Carbohydrate research, 2021-10, Vol.508, p.108399, Article 108399

2021

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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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Arabinofuranose 1,2,5-orthobenzoate as a single precursor of linear α(1 → 5)-linked oligoarabinofuranosides

Carbohydrate research, 2018-02, Vol.456, p.35-44

2018

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Bimodal concentration-dependent reactivity pattern of a glycosyl donor: Is the solution structure involved?

Carbohydrate research, 2017-01, Vol.437, p.28-35

2017

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Stereoselective sialylation with O-trifluoroacetylated thiosialosides: hydrogen bonding involved?

Carbohydrate research, 2017-11, Vol.451, p.12-28

2017

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A Concise Synthesis of the Repeating Unit of Capsular Polysaccharide Staphylococcus aureus Type 8

Organic letters, 2015-05, Vol.17 (10), p.2382-2384

2015

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The use of O-trifluoroacetyl protection and profound influence of the nature of glycosyl acceptor in benzyl-free arabinofuranosylation

Carbohydrate research, 2014-09, Vol.396, p.25-36

2014

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Formation of orthoester-linked d-arabinofuranose oligosaccharides and their isomerization into the corresponding glycosides

Tetrahedron letters, 2011-04, Vol.52 (15), p.1794-1796

2011

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Ring opening of acylated β- d-arabinofuranose 1,2,5-orthobenzoates with nucleophiles allows access to novel selectively-protected arabinofuranose building blocks

Carbohydrate research, 2011-01, Vol.346 (1), p.7-15

2011

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Convenient Synthesis and Purification of N-Trifluoroacetylated Neuraminic Acid Tetraol: A Key Precursor for the Synthesis of New Sialyl Donors Containing Labile O-Acyl Protecting Groups

Journal of carbohydrate chemistry, 2014-06, Vol.33 (5), p.213-224

2014

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Per-O-benzoyl-1,2-O-benzylidene derivatives of Pyranoses and Furanoses-Versatile Building Blocks for Oligosaccharide Synthesis

Carbohydrate Chemistry, 2018, Vol.4, p.141-150

1, 2018

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A Facile Synthesis of 1,3,4,6-Tetra-O-acetyl-2-deoxy-2-trifluoroacetamido-β-d-glucopyranose

Carbohydrate Chemistry, 2018, Vol.4, p.255-262

1, 2018

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Improved Large-Scale Synthesis of β-d-Arabinofuranose 1,2,5-Orthobenzoate

Carbohydrate Chemistry, 2015, p.196-203

2015

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Comparison of glycosyl donors: a supramer approach

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 photoactivable oligosaccharide derivatives from 1,2-cyclic carbamate building blocks and study of their interaction with carbohydrate-binding proteins

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

Arabinofuranose 1,2,5-orthobenzoate as a single precursor of linear α(1 → 5)-linked oligoarabinofuranosides

Bimodal concentration-dependent reactivity pattern of a glycosyl donor: Is the solution structure involved?

Stereoselective sialylation with O-trifluoroacetylated thiosialosides: hydrogen bonding involved?

A Concise Synthesis of the Repeating Unit of Capsular Polysaccharide Staphylococcus aureus Type 8

The use of O-trifluoroacetyl protection and profound influence of the nature of glycosyl acceptor in benzyl-free arabinofuranosylation

Formation of orthoester-linked d-arabinofuranose oligosaccharides and their isomerization into the corresponding glycosides

Ring opening of acylated β- d-arabinofuranose 1,2,5-orthobenzoates with nucleophiles allows access to novel selectively-protected arabinofuranose building blocks

Convenient Synthesis and Purification of N-Trifluoroacetylated Neuraminic Acid Tetraol: A Key Precursor for the Synthesis of New Sialyl Donors Containing Labile O-Acyl Protecting Groups

Per-O-benzoyl-1,2-O-benzylidene derivatives of Pyranoses and Furanoses-Versatile Building Blocks for Oligosaccharide Synthesis

A Facile Synthesis of 1,3,4,6-Tetra-O-acetyl-2-deoxy-2-trifluoroacetamido-β-d-glucopyranose

Improved Large-Scale Synthesis of β-d-Arabinofuranose 1,2,5-Orthobenzoate

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