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Characterization of the Isochromen-4-yl-gold(I) Intermediate in the Gold(I)-Catalyzed Glycosidation of Glycosyl ortho-Alkynylbenzoates and Enhancement of the Catalytic Efficiency Thereof

Angewandte Chemie International Edition, 2011-08, Vol.50 (36), p.8329-8332

International ed. in English, 2011

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Stereoselective gold(I)-catalyzed approach to the synthesis of complex α-glycosyl phosphosaccharides

Nature communications, 2022-01, Vol.13 (1), p.421-421, Article 421

2022

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Enantioselective Tandem Cyclization of Alkyne‐Tethered Indoles Using Cooperative Silver(I)/Chiral Phosphoric Acid Catalysis

Angewandte Chemie International Edition, 2017-09, Vol.56 (40), p.12206-12209

International ed. in English, 2017

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Highly Stereoselective β-Mannopyranosylation via the 1-α-Glycosyloxy-isochromenylium-4-gold(I) Intermediates

Chemistry : a European journal, 2015-06, Vol.21 (24), p.8771-8780

2015

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Highly Stereoselective [beta]-Mannopyranosylation via the 1-[alpha]-Glycosyloxy-isochromenylium-4-gold(I) Intermediates

Chemistry : a European journal, 2015-06, Vol.21 (24), p.8771

2015

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Mechanistic Insights into the Gold(I)-Catalyzed Activation of Glycosyl ortho-Alkynylbenzoates for Glycosidation

Journal of the American Chemical Society, 2013-12, Vol.135 (49), p.18396-18405

2013

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An Efficient Approach to the Synthesis of Nucleosides: Gold(I)-Catalyzed N-Glycosylation of Pyrimidines and Purines with Glycosyl ortho-Alkynyl Benzoates

Angewandte Chemie International Edition, 2011-05, Vol.50 (21), p.4933-4936

International ed. in English, 2011

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Inside Cover: Highly Stereoselective [beta]-Mannopyranosylation via the 1-[alpha]-Glycosyloxy-isochromenylium-4-gold(I) Intermediates

Chemistry : a European journal, 2015-06, Vol.21 (24), p.8642

2015

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Inside Cover: Highly Stereoselective β-Mannopyranosylation via the 1-α-Glycosyloxy-isochromenylium-4-gold(I) Intermediates (Chem. Eur. J. 24/2015)

Chemistry : a European journal, 2015-06, Vol.21 (24), p.8642-8642

2015

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A dramatic concentration effect on the stereoselectivity of N-glycosylation for the synthesis of 2'-deoxy-β-ribonucleosides

Chemical communications (Cambridge, England), 2012-07, Vol.48 (56), p.7097-7099

2012

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Chemoenzymatic Synthesis of Phosphosaccharides from Haemophilus parasuis Strains ER-6P (Serovar 15) and Nagasaki (Serovar 5)

Organic letters, 2024-10, Vol.26 (44), p.9580

2024

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Stereoselective synthesis of β-rhamnopyranosides via gold(I)-catalyzed glycosylation with 2-alkynyl-4-nitro-benzoate donors

Organic & biomolecular chemistry, 2016-02, Vol.14 (5), p.1536-1539

2016

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An Approach to the Synthesis of Electron-Rich and Hindered Esters and Its Application to the Synthesis of Acteoside

Organic letters, 2021-12, Vol.23 (23), p.9210-9215

2021

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An Anomeric Base‐Tolerant Ester of 8‐Alkynyl‐1‐naphthoate for Gold(I)‐Catalyzed Glycosylation Reaction

Chinese journal of chemistry, 2023-06, Vol.41 (11), p.1305-1312

2023

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Tetracyclic indolines as a novel class of β-lactam-selective resistance-modifying agent for MRSA

European journal of medicinal chemistry, 2017-01, Vol.125, p.130-142

2017

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Stereoselective synthesis of β-rhamnopyranosides via gold(i)-catalyzed glycosylation with 2-alkynyl-4-nitro-benzoate donorsElectronic supplementary information (ESI) available: Experimental procedures and spectral data. See DOI: 10.1039/c5ob02551f

2016-01

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A dramatic concentration effect on the stereoselectivity of N-glycosylation for the synthesis of 2′-deoxy-β-ribonucleosidesElectronic supplementary information (ESI) available: Experimental details, characterization data, and NMR spectra for all new compounds. The crystallographic data for compounds 5bβ (CCDC 865441) and 5dβ (CCDC 865440) can be obtained free of charge from the Cambridge Crystallographic Data Centre viawww.ccdc.cam.ac.uk/data_request/cif. For ESI and crystallographic data in CIF

2012-06

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A Polystyrene-Bound Triphenylphosphine Gold(I) Catalyst for the Glycosylation of Glycosyl ortho-Hexynylbenzoates

Asian journal of organic chemistry, 2015-10, Vol.4 (10), p.1034-1039

2015

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Characterization of the Isochromen-4-yl-gold(I) Intermediate in the Gold(I)-Catalyzed Glycosidation of Glycosyl ortho-Alkynylbenzoates and Enhancement of the Catalytic Efficiency Thereof

Angewandte Chemie, 2011-08, Vol.123 (36), p.8479-8482

2011

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Enantioselective Tandem Cyclization of Alkyne‐Tethered Indoles Using Cooperative Silver(I)/Chiral Phosphoric Acid Catalysis

Angewandte Chemie, 2017-09, Vol.129 (40), p.12374-12377

2017

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An Efficient Approach to the Synthesis of Nucleosides: Gold(I)-Catalyzed N-Glycosylation of Pyrimidines and Purines with Glycosyl ortho-Alkynyl Benzoates

Angewandte Chemie, 2011-05, Vol.123 (21), p.5035-5038

2011

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ChemInform Abstract: Stereoselective Synthesis of β‐Rhamnopyranosides via Gold(I)‐Catalyzed Glycosylation with 2‐Alkynyl‐4‐nitro‐benzoate Donors

ChemInform, 2016-05, Vol.47 (24), p.no-no

2016

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ChemInform Abstract: Stereoselective Synthesis of [beta]-Rhamnopyranosides via Gold(I)-Catalyzed Glycosylation with 2-Alkynyl-4-nitro-benzoate Donors

ChemInform, 2016-05, Vol.47 (24)

2016

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ChemInform Abstract: A Dramatic Concentration Effect on the Stereoselectivity of N-Glycosylation for the Synthesis of 2′-Deoxy-β-ribonucleosides

ChemInform, 2012-11, Vol.43 (45), p.no-no

2012

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ChemInform Abstract: A Dramatic Concentration Effect on the Stereoselectivity of N-Glycosylation for the Synthesis of 2'-Deoxy-[beta]-ribonucleosides

ChemInform, 2012-11, Vol.43 (45), p.no

2012

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Characterization of the Isochromen-4-yl-gold(I) Intermediate in the Gold(I)-Catalyzed Glycosidation of Glycosyl ortho-Alkynylbenzoates and Enhancement of the Catalytic Efficiency Thereof

Stereoselective gold(I)-catalyzed approach to the synthesis of complex α-glycosyl phosphosaccharides

Enantioselective Tandem Cyclization of Alkyne‐Tethered Indoles Using Cooperative Silver(I)/Chiral Phosphoric Acid Catalysis

Highly Stereoselective β-Mannopyranosylation via the 1-α-Glycosyloxy-isochromenylium-4-gold(I) Intermediates

Highly Stereoselective [beta]-Mannopyranosylation via the 1-[alpha]-Glycosyloxy-isochromenylium-4-gold(I) Intermediates

Mechanistic Insights into the Gold(I)-Catalyzed Activation of Glycosyl ortho-Alkynylbenzoates for Glycosidation

An Efficient Approach to the Synthesis of Nucleosides: Gold(I)-Catalyzed N-Glycosylation of Pyrimidines and Purines with Glycosyl ortho-Alkynyl Benzoates

Inside Cover: Highly Stereoselective [beta]-Mannopyranosylation via the 1-[alpha]-Glycosyloxy-isochromenylium-4-gold(I) Intermediates

Inside Cover: Highly Stereoselective β-Mannopyranosylation via the 1-α-Glycosyloxy-isochromenylium-4-gold(I) Intermediates (Chem. Eur. J. 24/2015)

A dramatic concentration effect on the stereoselectivity of N-glycosylation for the synthesis of 2'-deoxy-β-ribonucleosides

Chemoenzymatic Synthesis of Phosphosaccharides from Haemophilus parasuis Strains ER-6P (Serovar 15) and Nagasaki (Serovar 5)

Stereoselective synthesis of β-rhamnopyranosides via gold(I)-catalyzed glycosylation with 2-alkynyl-4-nitro-benzoate donors

An Approach to the Synthesis of Electron-Rich and Hindered Esters and Its Application to the Synthesis of Acteoside

An Anomeric Base‐Tolerant Ester of 8‐Alkynyl‐1‐naphthoate for Gold(I)‐Catalyzed Glycosylation Reaction

Tetracyclic indolines as a novel class of β-lactam-selective resistance-modifying agent for MRSA

Stereoselective synthesis of β-rhamnopyranosides via gold(i)-catalyzed glycosylation with 2-alkynyl-4-nitro-benzoate donorsElectronic supplementary information (ESI) available: Experimental procedures and spectral data. See DOI: 10.1039/c5ob02551f

A Polystyrene-Bound Triphenylphosphine Gold(I) Catalyst for the Glycosylation of Glycosyl ortho-Hexynylbenzoates

Characterization of the Isochromen-4-yl-gold(I) Intermediate in the Gold(I)-Catalyzed Glycosidation of Glycosyl ortho-Alkynylbenzoates and Enhancement of the Catalytic Efficiency Thereof

Enantioselective Tandem Cyclization of Alkyne‐Tethered Indoles Using Cooperative Silver(I)/Chiral Phosphoric Acid Catalysis

An Efficient Approach to the Synthesis of Nucleosides: Gold(I)-Catalyzed N-Glycosylation of Pyrimidines and Purines with Glycosyl ortho-Alkynyl Benzoates

ChemInform Abstract: Stereoselective Synthesis of β‐Rhamnopyranosides via Gold(I)‐Catalyzed Glycosylation with 2‐Alkynyl‐4‐nitro‐benzoate Donors

ChemInform Abstract: Stereoselective Synthesis of [beta]-Rhamnopyranosides via Gold(I)-Catalyzed Glycosylation with 2-Alkynyl-4-nitro-benzoate Donors

ChemInform Abstract: A Dramatic Concentration Effect on the Stereoselectivity of N-Glycosylation for the Synthesis of 2′-Deoxy-β-ribonucleosides

ChemInform Abstract: A Dramatic Concentration Effect on the Stereoselectivity of N-Glycosylation for the Synthesis of 2'-Deoxy-[beta]-ribonucleosides

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