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Versatile synthesis of 2′-amino-2′-deoxyuridine derivatives with a 2′-amino group carrying linkers possessing a reactive terminal functionality

Tetrahedron, 2016-09, Vol.72 (36), p.5626-5632

2016

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Synthesis and anti-tuberculosis activity of N-aryl- C-nitroazoles

European journal of medicinal chemistry, 2004-10, Vol.39 (10), p.849-853

2004

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Identification of 8-methyladenosine as the modification catalyzed by the radical SAM methyltransferase Cfr that confers antibiotic resistance in bacteria

RNA (Cambridge), 2009-02, Vol.15 (2), p.327-336

2009

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New approach for the synthesis of 1-aryl- and 1-heteroaryl-5-nitrouracil derivatives

Tetrahedron, 2007-03, Vol.63 (13), p.2859-2864

2007

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A convenient method for N-1 arylation of uracil derivatives

Tetrahedron letters, 2006-07, Vol.47 (27), p.4653-4657

2006

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Abstract 1281: Development and characterization of small molecule HPK1 inhibitors

Cancer research (Chicago, Ill.), 2021-07, Vol.81 (13_Supplement), p.1281-1281

2021

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Synthesis of amide and sulfonamide substituted N-aryl 6-aminoquinoxalines as PFKFB3 inhibitors with improved physicochemical properties

Bioorganic & medicinal chemistry letters, 2019-02, Vol.29 (4), p.646-653

2019

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Discovery and Structure–Activity Relationships of N‐Aryl 6‐Aminoquinoxalines as Potent PFKFB3 Kinase Inhibitors

ChemMedChem, 2019-01, Vol.14 (1), p.169-181

2019

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Hybrids of Iron-Filled Multiwall Carbon Nanotubes and Anticancer Agents as Potential Magnetic Drug Delivery Systems: In Vitro Studies against Human Melanoma, Colon Carcinoma, and Colon Adenocarcinoma

Journal of nanomaterials, 2017-01, Vol.2017, p.1-13

2017

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Abstract 449: Discovery of novel MTA-cooperative PRMT5 inhibitors as targeted therapeutics for MTAP -deleted cancers

Cancer research (Chicago, Ill.), 2023-04, Vol.83 (7_Supplement), p.449-449

2023

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Abstract 1806: Discovery of novel MTA-cooperative PRMT5 inhibitors as a targeted therapeutics for MTAP deleted cancers

Cancer research (Chicago, Ill.), 2022-06, Vol.82 (12_Supplement), p.1806-1806

2022

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N-Functionalization of uracil derivatives: synthesis of chiral 2-(3-methyl-5-nitro-2,4-dioxo-3,4-dihydropyrimidin-1(2 H)-yl)alkanoic acids and their methyl esters

Tetrahedron: asymmetry, 2005-06, Vol.16 (12), p.2107-2112

2005

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Synthesis of 2-deoxy-2-(4-nitroimidazol-1-yl)- d-alditols

Carbohydrate research, 2005-05, Vol.340 (7), p.1379-1385

2005

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Synthesis of 1-(dihydroxypropyl)-5-substituted uracils

Tetrahedron letters, 2003-09, Vol.44 (39), p.7291-7293

2003

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Synthesis and Biophysical Properties of Oligodeoxynucleotides Containing 2′-Deoxy-5-(4-nitro-1H-imidazol-1-yl)-β-D-uridine and 2′-Deoxy-5-(1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl)-β-D-uridine Monomers

Chemistry & biodiversity, 2010-02, Vol.7 (2), p.350-362

2010

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Novel transformation of 5-cyanouracil derivatives

Tetrahedron letters, 2004-10, Vol.45 (43), p.8007-8009

2004

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New Approach for the Synthesis of 1-Aryl- and 1-Heteroaryl-5-nitrouracil Derivatives

ChemInform, 2007-07, Vol.38 (27), p.no-no

2007

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A Convenient Method for N-1 Arylation of Uracil Derivatives

ChemInform, 2006-10, Vol.37 (41), p.no-no

2006

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ChemInform Abstract: Michael-Type Addition as a Convenient Method for Regioselective N-Alkylation of Ambident Uracils

ChemInform, 2010-07, Vol.41 (30), p.no-no

2010

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N-Functionalization of Uracil Derivatives: Synthesis of Chiral 2-(3-Methyl-5-nitro-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)alkanoic Acids and Their Methyl Esters

ChemInform, 2005-11, Vol.36 (44), p.no-no

2005

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ChemInform Abstract: Uracil as a Target for Nucleophilic and Electrophilic Reagents

ChemInform, 2009-08, Vol.40 (34), p.no-no

2009

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Synthesis of 1-(Dihydroxypropyl)-5-Substituted Uracils

ChemInform, 2004-01, Vol.35 (1), p.no-no

2004

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Synthesis and Antituberculosis Activity of N-Aryl-C-nitroazoles

ChemInform, 2005-03, Vol.36 (11), p.no-no

2005

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Novel Transformation of 5-Cyanouracil Derivatives

ChemInform, 2005-02, Vol.36 (6), p.no-no

2005

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Uracil Derivatives
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Amination, N‐alkylation, N‐arylation
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Versatile synthesis of 2′-amino-2′-deoxyuridine derivatives with a 2′-amino group carrying linkers possessing a reactive terminal functionality

Synthesis and anti-tuberculosis activity of N-aryl- C-nitroazoles

Identification of 8-methyladenosine as the modification catalyzed by the radical SAM methyltransferase Cfr that confers antibiotic resistance in bacteria

Discovery of 5-{2-[5-Chloro-2-(5-ethoxyquinoline-8-sulfonamido)phenyl]ethynyl}-4-methoxypyridine-2-carboxylic Acid, a Highly Selective in Vivo Useable Chemical Probe to Dissect MCT4 Biology

New approach for the synthesis of 1-aryl- and 1-heteroaryl-5-nitrouracil derivatives

A convenient method for N-1 arylation of uracil derivatives

Abstract 1281: Development and characterization of small molecule HPK1 inhibitors

Synthesis of amide and sulfonamide substituted N-aryl 6-aminoquinoxalines as PFKFB3 inhibitors with improved physicochemical properties

Discovery and Structure–Activity Relationships of N‐Aryl 6‐Aminoquinoxalines as Potent PFKFB3 Kinase Inhibitors

Hybrids of Iron-Filled Multiwall Carbon Nanotubes and Anticancer Agents as Potential Magnetic Drug Delivery Systems: In Vitro Studies against Human Melanoma, Colon Carcinoma, and Colon Adenocarcinoma

Abstract 449: Discovery of novel MTA-cooperative PRMT5 inhibitors as targeted therapeutics for MTAP -deleted cancers

Abstract 1806: Discovery of novel MTA-cooperative PRMT5 inhibitors as a targeted therapeutics for MTAP deleted cancers

N-Functionalization of uracil derivatives: synthesis of chiral 2-(3-methyl-5-nitro-2,4-dioxo-3,4-dihydropyrimidin-1(2 H)-yl)alkanoic acids and their methyl esters

Synthesis of 2-deoxy-2-(4-nitroimidazol-1-yl)- d-alditols

Synthesis of 1-(dihydroxypropyl)-5-substituted uracils

Synthesis and Biophysical Properties of Oligodeoxynucleotides Containing 2′-Deoxy-5-(4-nitro-1H-imidazol-1-yl)-β-D-uridine and 2′-Deoxy-5-(1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl)-β-D-uridine Monomers

Novel transformation of 5-cyanouracil derivatives

New Approach for the Synthesis of 1-Aryl- and 1-Heteroaryl-5-nitrouracil Derivatives

A Convenient Method for N-1 Arylation of Uracil Derivatives

ChemInform Abstract: Michael-Type Addition as a Convenient Method for Regioselective N-Alkylation of Ambident Uracils

N-Functionalization of Uracil Derivatives: Synthesis of Chiral 2-(3-Methyl-5-nitro-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)alkanoic Acids and Their Methyl Esters

ChemInform Abstract: Uracil as a Target for Nucleophilic and Electrophilic Reagents

Synthesis of 1-(Dihydroxypropyl)-5-Substituted Uracils

Synthesis and Antituberculosis Activity of N-Aryl-C-nitroazoles

Novel Transformation of 5-Cyanouracil Derivatives

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