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Specific Inhibitors of HIV Capsid Assembly Binding to the C‑Terminal Domain of the Capsid Protein: Evaluation of 2‑Arylquinazolines as Potential Antiviral Compounds

Journal of medicinal chemistry, 2016-01, Vol.59 (2), p.545-558

2016

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Modular Stereoselective Synthesis of (1→2)-C-Glycosides based on the sp2-sp3 Suzuki-Miyaura Reaction

Chemistry : a European journal, 2015-05, Vol.21 (19), p.7043-7047

2015

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MOP and EE Protecting Groups in Synthesis of α- or β‑Naphthyl‑C‑Glycosides from Glycals

ACS omega, 2018-07, Vol.3 (7), p.7875-7887

2018

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Limitations in the description of conformational preferences of C-disaccharides: The (1 → 3)-C-mannobiose case

Carbohydrate research, 2017-11, Vol.451, p.42-50

2017

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Nonhydrolyzable C-disaccharides, a new class of DC-SIGN ligands

Carbohydrate research, 2016-11, Vol.435, p.7-18

2016

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Cross-metathesis reaction of α- and β-vinyl C-glycosides with alkenes

Beilstein journal of organic chemistry, 2015-08, Vol.11 (1), p.1392-1397

2015

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Cross-Coupling Reaction of Saccharide-Based Alkenyl Boronic Acids with Aryl Halides: The Synthesis of Bergenin

Chemistry : a European journal, 2014-04, Vol.20 (15), p.4414-4419

2014

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On the origin of the electronic and magnetic circular dichroism of naphthyl C-glycosides: Anomeric configuration

Carbohydrate research, 2024-01, Vol.535, p.109021-109021, Article 109021

2024

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Front Cover: Facile Approach to C‐Glucosides by Using a Protecting‐Group‐Free Hiyama Cross‐Coupling Reaction: High‐Yielding Dapagliflozin Synthesis (Chem. Eur. J. 41/2021)

Chemistry : a European journal, 2021-07, Vol.27 (41), p.10484-10484

2021

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The synthesis and characterization of electron-poor glycosylamines and derived glycosylamides

Carbohydrate research, 2024-02, Vol.536, p.109023-109023, Article 109023

2024

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Facile Approach to C‐Glucosides by Using a Protecting‐Group‐Free Hiyama Cross‐Coupling Reaction: High‐Yielding Dapagliflozin Synthesis

Chemistry : a European journal, 2021-07, Vol.27 (41), p.10583-10588

2021

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Unlocking the Hydrolytic Mechanism of GH92 α‐1,2‐Mannosidases: Computation Inspires the use of C‐Glycosides as Michaelis Complex Mimics

Chemistry : a European journal, 2022-03, Vol.28 (14), p.e202200148-n/a

2022

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Facile Approach to C‐Glucosides by Using a Protecting‐Group‐Free Hiyama Cross‐Coupling Reaction: High‐Yielding Dapagliflozin Synthesis

Chemistry : a European journal, 2021-07, Vol.27 (41), p.10488-10488

2021

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Modular Stereoselective Synthesis of (1→2)-C-Glycosides based on the sp(2) -sp(3) Suzuki-Miyaura Reaction

Chemistry : a European journal, 2015-05, Vol.21 (19), p.7043-7047

2015

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Straightforward synthesis of protected 2-hydroxyglycals by chlorination-dehydrochlorination of carbohydrate hemiacetals

Carbohydrate research, 2020-10, Vol.496, p.108086-108086, Article 108086

2020

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Silicon-bridged (1→1)-disaccharides: an umpoled glycomimetic scaffold

Organic & biomolecular chemistry, 2022-10, Vol.2 (38), p.7613-7621

2022

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Selection of Galectin‐Binding Ligands from Synthetic Glycopeptide Libraries

ChemPlusChem (Weinheim, Germany), 2024-07, Vol.89 (7), p.e202300567-n/a

2024

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Modular Stereoselective Synthesis of (1→2)‐ C ‐Glycosides based on the sp 2 –sp 3 Suzuki–Miyaura Reaction

Chemistry : a European journal, 2015-05, Vol.21 (19), p.7043-7047

2015

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Modular Stereoselective Synthesis of (1 arrow right 2)-C-Glycosides based on the sp super(2)-sp super(3) Suzuki-Miyaura Reaction

Chemistry : a European journal, 2015-05, Vol.21 (19), p.7043-7047

2015

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Fucosylated inhibitors of recently identified bangle lectin from Photorhabdus asymbiotica

Scientific reports, 2019-10, Vol.9 (1), p.14904-12, Article 14904

2019

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Polyvalent C-glycomimetics based on l-fucose or d-mannose as potent DC-SIGN antagonists

Organic & biomolecular chemistry, 2017-05, Vol.15 (18), p.3995-4004

2017

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Lectin PLL3, a Novel Monomeric Member of the Seven-Bladed β-Propeller Lectin Family

Molecules (Basel, Switzerland), 2019-12, Vol.24 (24), p.4540

2019

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Stereoselective preparation of four 3-C-mannosylated D- and L-glucals from a single starting compound: Strategies for the Synthesis of Tetrahydropyran-Containing Natural Products

Tetrahedron, 2011, Vol.67 (27-28)

2011

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Polyvalent C-glycomimetics based on l-fucose or d-mannose as potent DC-SIGN antagonistsElectronic supplementary information (ESI) available: MS and NMR characterization of new compounds, SPR sensorgrams, inhibition curves, and IC50 values. See DOI: 10.1039/c7ob00322f

2017-05

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Synthesis and evaluation of 2-pyridinylpyrimidines as inhibitors of HIV-1 structural protein assembly

Bioorganic & medicinal chemistry letters, 2016-08, Vol.26 (15), p.3487-3490

2016

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Specific Inhibitors of HIV Capsid Assembly Binding to the C‑Terminal Domain of the Capsid Protein: Evaluation of 2‑Arylquinazolines as Potential Antiviral Compounds

Modular Stereoselective Synthesis of (1→2)-C-Glycosides based on the sp2-sp3 Suzuki-Miyaura Reaction

MOP and EE Protecting Groups in Synthesis of α- or β‑Naphthyl‑C‑Glycosides from Glycals

Limitations in the description of conformational preferences of C-disaccharides: The (1 → 3)-C-mannobiose case

Nonhydrolyzable C-disaccharides, a new class of DC-SIGN ligands

Cross-metathesis reaction of α- and β-vinyl C-glycosides with alkenes

Cross-Coupling Reaction of Saccharide-Based Alkenyl Boronic Acids with Aryl Halides: The Synthesis of Bergenin

On the origin of the electronic and magnetic circular dichroism of naphthyl C-glycosides: Anomeric configuration

Front Cover: Facile Approach to C‐Glucosides by Using a Protecting‐Group‐Free Hiyama Cross‐Coupling Reaction: High‐Yielding Dapagliflozin Synthesis (Chem. Eur. J. 41/2021)

The synthesis and characterization of electron-poor glycosylamines and derived glycosylamides

Facile Approach to C‐Glucosides by Using a Protecting‐Group‐Free Hiyama Cross‐Coupling Reaction: High‐Yielding Dapagliflozin Synthesis

Unlocking the Hydrolytic Mechanism of GH92 α‐1,2‐Mannosidases: Computation Inspires the use of C‐Glycosides as Michaelis Complex Mimics

Facile Approach to C‐Glucosides by Using a Protecting‐Group‐Free Hiyama Cross‐Coupling Reaction: High‐Yielding Dapagliflozin Synthesis

Modular Stereoselective Synthesis of (1→2)-C-Glycosides based on the sp(2) -sp(3) Suzuki-Miyaura Reaction

Straightforward synthesis of protected 2-hydroxyglycals by chlorination-dehydrochlorination of carbohydrate hemiacetals

Silicon-bridged (1→1)-disaccharides: an umpoled glycomimetic scaffold

Selection of Galectin‐Binding Ligands from Synthetic Glycopeptide Libraries

Modular Stereoselective Synthesis of (1→2)‐ C ‐Glycosides based on the sp 2 –sp 3 Suzuki–Miyaura Reaction

Modular Stereoselective Synthesis of (1 arrow right 2)-C-Glycosides based on the sp super(2)-sp super(3) Suzuki-Miyaura Reaction

Fucosylated inhibitors of recently identified bangle lectin from Photorhabdus asymbiotica

Polyvalent C-glycomimetics based on l-fucose or d-mannose as potent DC-SIGN antagonists

Lectin PLL3, a Novel Monomeric Member of the Seven-Bladed β-Propeller Lectin Family

Stereoselective preparation of four 3-C-mannosylated D- and L-glucals from a single starting compound: Strategies for the Synthesis of Tetrahydropyran-Containing Natural Products

Polyvalent C-glycomimetics based on l-fucose or d-mannose as potent DC-SIGN antagonistsElectronic supplementary information (ESI) available: MS and NMR characterization of new compounds, SPR sensorgrams, inhibition curves, and IC50 values. See DOI: 10.1039/c7ob00322f

Synthesis and evaluation of 2-pyridinylpyrimidines as inhibitors of HIV-1 structural protein assembly

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