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Discovery of an L‐like Configuration for 3’‐Fluoro‐5’‐norcarbonucleoside Phosphonates as Potent Anti‐HIV Agents

ChemMedChem, 2022-10, Vol.17 (20), p.e202200377-n/a

2022

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Second‐Generation CD73 Inhibitors Based on a 4,6‐Biaryl‐2‐thiopyridine Scaffold

ChemMedChem, 2023-04, Vol.18 (7), p.e202200594-n/a

2023

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Synthesis of Substituted 5′‐Aminoadenosine Derivatives and Evaluation of Their Inhibitory Potential toward CD73

ChemMedChem, 2019-08, Vol.14 (15), p.1431-1443

2019

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An Eco‐Friendly and Efficient Photoinduced Coupling of Alkenes and Alkynes with H‐Phosphinates and Other P(O)H Derivatives Under Free‐Radical Conditions

European journal of organic chemistry, 2017-07, Vol.2017 (26), p.3850-3855

2017

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Synthesis and Antiviral Evaluation of 3′‐Fluoro‐4′‐modified‐5′‐norcarbocyclic Nucleoside Phosphonates

ChemMedChem, 2019-03, Vol.14 (5), p.522-526

2019

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Synthesis and Antiviral Evaluation of 3'-Fluoro-5'-norcarbocyclic Nucleoside Phosphonates Bearing Uracil and Cytosine as Potential Antiviral Agents

Molecules (Basel, Switzerland), 2020-08, Vol.25 (16), p.3708

2020

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Probing the reactivity of H-phosphonate derivatives for the hydrophosphonylation of various alkenes and alkynes under free-radical conditions

New journal of chemistry, 2016, Vol.40 (6), p.5318-5324

2016

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2‑(Substituted amino)-8-azachromones from 4,6-Diaryl-2-pyridones: A Synthetic Strategy toward Compounds of Broad Structural Diversity

Journal of organic chemistry, 2020-09, Vol.85 (18), p.11778-11793

2020

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Purine containing carbonucleoside phosphonate analogues as novel chemotype for Plasmodium falciparum Inhibition

European journal of medicinal chemistry, 2023-10, Vol.258, p.115581-115581, Article 115581

2023

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Synthesis of 3′-halo-5′-norcarbocyclic nucleoside phosphonates as potent anti-HIV agents

European journal of medicinal chemistry, 2018-04, Vol.150, p.642-654

2018

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4-Substituted-1,2,3-triazolo nucleotide analogues as CD73 inhibitors, their synthesis, in vitro screening, kinetic and in silico studies

Bioorganic chemistry, 2021-02, Vol.107, p.104577-104577, Article 104577

2021

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Rapid synthesis of carbonucleoside phophonate analogues as potential antiviral agents via a hydrophosphonylation reaction of ethynyl carbocyclic precursors

New journal of chemistry, 2018, Vol.42 (2), p.974-979

2018

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Synthesis of novel 3′-methyl-5′-norcarbocyclic nucleoside phosphonates as potential anti-HIV agents

Tetrahedron, 2013-03, Vol.69 (9), p.2131-2136

2013

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Chemoenzymatic Taxanes Approach Using Both Enantiomers of the Same Building Block. 2. Taxol CD Ring Unit

Journal of organic chemistry, 2005-04, Vol.70 (9), p.3484-3489

2005

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Synthesis of {[5-(adenin-9-yl)-2-furyl]methoxy}methyl phosphonic acid and evaluations against human adenylate kinases

Bioorganic & medicinal chemistry letters, 2014-09, Vol.24 (17), p.4227-4230

2014

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Synthesis of the natural enantiomer of neplanocin B

Bioorganic chemistry, 2010-12, Vol.38 (6), p.275-278

2010

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Probing of PSE acetal protection for nucleoside chemistry

Tetrahedron letters, 2007-05, Vol.48 (22), p.3851-3854

2007

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Characterization of a self-assembled monolayer based on a calix[4]crown-5 derivate: fabrication of a chemical sensor sensitive to calcium

Journal of nanoscience and nanotechnology, 2010-01, Vol.10 (1), p.413-420

2010

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First Enantioselective Synthesis and Absolute Stereochemistry Assignment of New Monocyclic Sesquiterpenes from Artemisia chamaemelifolia

Journal of organic chemistry, 2003-06, Vol.68 (13), p.5407-5410

2003

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A stereocontrolled approach towards highly oxygenated taxane C and CD-ring precursors

Tetrahedron letters, 2002-04, Vol.43 (15), p.2757-2760

2002

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Enantioselective Taxanes Approach Using Both Enantiomers of the Same Building-Block. Part 1: Taxol® A-Ring Subunit

Synlett, 2002, Vol.2002 (8), p.1261-1264

2002

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Rapid synthesis of carbonucleoside phophonate analogues as potential antiviral agents via a hydrophosphonylation reaction of ethynyl carbocyclic precursorsElectronic supplementary information (ESI) available: Spectra of selected compounds. See DOI: 10.1039/c7nj03991c

2018-01

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First enantioselective synthesis of (-)-neplanocin B

Nucleic Acids Symposium Series, 2008-09, Vol.52 (1), p.545-546

2008

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Probing the reactivity of H-phosphonate derivatives for the hydrophosphonylation of various alkenes and alkynes under free-radical conditionsElectronic supplementary information (ESI) available: Spectra for all compounds. See DOI: 10.1039/c6nj00123h

2016-06

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ChemInform Abstract: Probing the Reactivity of H‐Phosphonate Derivatives for the Hydrophosphonylation of Various Alkenes and Alkynes under Free‐Radical Conditions

ChemInform, 2016-09, Vol.47 (42), p.no-no

2016

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Discovery of an L‐like Configuration for 3’‐Fluoro‐5’‐norcarbonucleoside Phosphonates as Potent Anti‐HIV Agents

Second‐Generation CD73 Inhibitors Based on a 4,6‐Biaryl‐2‐thiopyridine Scaffold

Synthesis of Substituted 5′‐Aminoadenosine Derivatives and Evaluation of Their Inhibitory Potential toward CD73

An Eco‐Friendly and Efficient Photoinduced Coupling of Alkenes and Alkynes with H‐Phosphinates and Other P(O)H Derivatives Under Free‐Radical Conditions

Synthesis and Antiviral Evaluation of 3′‐Fluoro‐4′‐modified‐5′‐norcarbocyclic Nucleoside Phosphonates

Synthesis and Antiviral Evaluation of 3'-Fluoro-5'-norcarbocyclic Nucleoside Phosphonates Bearing Uracil and Cytosine as Potential Antiviral Agents

Probing the reactivity of H-phosphonate derivatives for the hydrophosphonylation of various alkenes and alkynes under free-radical conditions

2‑(Substituted amino)-8-azachromones from 4,6-Diaryl-2-pyridones: A Synthetic Strategy toward Compounds of Broad Structural Diversity

Purine containing carbonucleoside phosphonate analogues as novel chemotype for Plasmodium falciparum Inhibition

Synthesis of 3′-halo-5′-norcarbocyclic nucleoside phosphonates as potent anti-HIV agents

4-Substituted-1,2,3-triazolo nucleotide analogues as CD73 inhibitors, their synthesis, in vitro screening, kinetic and in silico studies

Rapid synthesis of carbonucleoside phophonate analogues as potential antiviral agents via a hydrophosphonylation reaction of ethynyl carbocyclic precursors

Synthesis of novel 3′-methyl-5′-norcarbocyclic nucleoside phosphonates as potential anti-HIV agents

Chemoenzymatic Taxanes Approach Using Both Enantiomers of the Same Building Block. 2. Taxol CD Ring Unit

Synthesis of {[5-(adenin-9-yl)-2-furyl]methoxy}methyl phosphonic acid and evaluations against human adenylate kinases

Synthesis of the natural enantiomer of neplanocin B

Probing of PSE acetal protection for nucleoside chemistry

Characterization of a self-assembled monolayer based on a calix[4]crown-5 derivate: fabrication of a chemical sensor sensitive to calcium

First Enantioselective Synthesis and Absolute Stereochemistry Assignment of New Monocyclic Sesquiterpenes from Artemisia chamaemelifolia

A stereocontrolled approach towards highly oxygenated taxane C and CD-ring precursors

Enantioselective Taxanes Approach Using Both Enantiomers of the Same Building-Block. Part 1: Taxol® A-Ring Subunit

Rapid synthesis of carbonucleoside phophonate analogues as potential antiviral agents via a hydrophosphonylation reaction of ethynyl carbocyclic precursorsElectronic supplementary information (ESI) available: Spectra of selected compounds. See DOI: 10.1039/c7nj03991c

First enantioselective synthesis of (-)-neplanocin B

Probing the reactivity of H-phosphonate derivatives for the hydrophosphonylation of various alkenes and alkynes under free-radical conditionsElectronic supplementary information (ESI) available: Spectra for all compounds. See DOI: 10.1039/c6nj00123h

ChemInform Abstract: Probing the Reactivity of H‐Phosphonate Derivatives for the Hydrophosphonylation of Various Alkenes and Alkynes under Free‐Radical Conditions

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