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Selective Inhibitors of Cyclin G Associated Kinase (GAK) as Anti-Hepatitis C Agents

Journal of medicinal chemistry, 2015-04, Vol.58 (8), p.3393-3410

2015

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Isothiazolo[4,3- b ]pyridines as inhibitors of cyclin G associated kinase : synthesis, structure-activity relationship studies and antiviral activity

MedChemComm, 2015-01, Vol.6 (9), p.1666-1672

2015

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The synthesis of piperidine nucleoside analogs—a comparison of several methods to access the introduction of nucleobases

Tetrahedron, 2011-02, Vol.67 (7), p.1485-1500

2011

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Fluorescent 6-hydroxy- and 6,7-dihydroxy-4-trifluoro-methylcarbostyrils and formation of o-carboxymethylated derivatives via o-succinimide esters

Journal of heterocyclic chemistry, 2008-01, Vol.45 (1), p.165-172

2008

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Synthesis of coumarin–nucleoside conjugates via Huisgen 1,3-dipolar cycloaddition

Tetrahedron, 2007-01, Vol.63 (2), p.312-320

2007

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A convenient, high-yield synthesis of 1-substituted uracil and thymine derivatives

Tetrahedron, 2009-10, Vol.65 (41), p.8513-8523

2009

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Discovery of Dual Death-Associated Protein Related Apoptosis Inducing Protein Kinase 1 and 2 Inhibitors by a Scaffold Hopping Approach

Journal of medicinal chemistry, 2014-09, Vol.57 (18), p.7624-7643

2014

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Mechanism of the Isotopic Exchange Reaction of the 5-H Hydrogen of Uracil Derivatives in Water and Nonprotic Solvents

European Journal of Organic Chemistry, 2011-02, Vol.2011 (4), p.777-785

2011

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Selective inhibitors of Cyclin-G associated kinase (GAK) as anti-HCV agents

Journal of medicinal chemistry, 2015-04, Vol.58 (8), p.3393-3410

2015

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Characterization of suspected dermal fillers containing hyaluronic acid

Analytical methods, 2017-07, Vol.9 (28), p.4175-4183

2017

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Isothiazolo[4,3-b]pyridines as inhibitors of cyclin G associated kinase: synthesis, structure-activity relationship studies and antiviral activityElectronic supplementary information (ESI) available. See DOI: 10.1039/c5md00229j

2015-09

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One-pot build-up procedure for the synthesis of variously substituted purine derivatives

RSC advances, 2012, Vol.2 (17), p.6970

2012

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Lipophosphonoxins: New Modular Molecular Structures with Significant Antibacterial Properties

Journal of medicinal chemistry, 2011-11, Vol.54 (22), p.7884-7898

2011

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Nucleoside Phosphonic Acids in Thymidine Phosphorylase Inhibition: Structure - Activity Relationship

Nucleic Acids Symposium Series, 2008, Vol.52 (1), p.665-666

2008

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Piperidine nucleosides and nucleotides

Nucleic Acids Symposium Series, 2008, Vol.52 (1), p.587-587

2008

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ChemInform Abstract: One-Pot Build-Up Procedure for the Synthesis of Variously Substituted Purine Derivatives

ChemInform, 2012-12, Vol.43 (49), p.no-no

2012

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Isotopic Exchange of Hydrogen at C‐5 in Pyrimidine Derivatives: Tautomers with an sp3‐Hybridised C‐5 Carbon Atom

European Journal of Organic Chemistry, 2009, Vol.2009 (24), p.4117-4122

2009

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Pyrrolidine analogues of nucleosides and nucleotides

Nucleic Acids Symposium Series, 2008, Vol.52 (1), p.577-578

2008

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ChemInform Abstract: A Convenient, High-Yield Synthesis of 1-Substituted Uracil and Thymine Derivatives

ChemInform, 2010-02, Vol.41 (6), p.no-no

2010

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Isotopic Exchange of Hydrogen at C‐5 in Pyrimidine Derivatives: Tautomers with an sp 3 ‐Hybridised C‐5 Carbon Atom

European journal of organic chemistry, 2009-08, Vol.2009 (24), p.4117-4122

2009

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Selective Inhibitors of Cyclin G Associated Kinase (GAK) as Anti-Hepatitis C Agents

Isothiazolo[4,3- b ]pyridines as inhibitors of cyclin G associated kinase : synthesis, structure-activity relationship studies and antiviral activity

The synthesis of piperidine nucleoside analogs—a comparison of several methods to access the introduction of nucleobases

Fluorescent 6-hydroxy- and 6,7-dihydroxy-4-trifluoro-methylcarbostyrils and formation of o-carboxymethylated derivatives via o-succinimide esters

Synthesis of coumarin–nucleoside conjugates via Huisgen 1,3-dipolar cycloaddition

A convenient, high-yield synthesis of 1-substituted uracil and thymine derivatives

Discovery of Dual Death-Associated Protein Related Apoptosis Inducing Protein Kinase 1 and 2 Inhibitors by a Scaffold Hopping Approach

Mechanism of the Isotopic Exchange Reaction of the 5-H Hydrogen of Uracil Derivatives in Water and Nonprotic Solvents

Selective inhibitors of Cyclin-G associated kinase (GAK) as anti-HCV agents

Characterization of suspected dermal fillers containing hyaluronic acid

Isothiazolo[4,3-b]pyridines as inhibitors of cyclin G associated kinase: synthesis, structure-activity relationship studies and antiviral activityElectronic supplementary information (ESI) available. See DOI: 10.1039/c5md00229j

One-pot build-up procedure for the synthesis of variously substituted purine derivatives

Lipophosphonoxins: New Modular Molecular Structures with Significant Antibacterial Properties

Nucleoside Phosphonic Acids in Thymidine Phosphorylase Inhibition: Structure - Activity Relationship

Piperidine nucleosides and nucleotides

ChemInform Abstract: One-Pot Build-Up Procedure for the Synthesis of Variously Substituted Purine Derivatives

Isotopic Exchange of Hydrogen at C‐5 in Pyrimidine Derivatives: Tautomers with an sp3‐Hybridised C‐5 Carbon Atom

Pyrrolidine analogues of nucleosides and nucleotides

ChemInform Abstract: A Convenient, High-Yield Synthesis of 1-Substituted Uracil and Thymine Derivatives

Isotopic Exchange of Hydrogen at C‐5 in Pyrimidine Derivatives: Tautomers with an sp 3 ‐Hybridised C‐5 Carbon Atom

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