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Nucleosides and Oligonucleotides with Diynyl Side Chains: Base Pairing and Functionalization of 2′-Deoxyuridine Derivatives by the Copper(I)-Catalyzed AlkyneAzide 'Click' Cycloaddition

Helvetica chimica acta, 2007-03, Vol.90 (3), p.535-552

2007

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MPX-004 and MPX-007: New Pharmacological Tools to Study the Physiology of NMDA Receptors Containing the GluN2A Subunit

PloS one, 2016-02, Vol.11 (2), p.e0148129-e0148129

2016

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5‑Arylidenethioxothiazolidinones as Inhibitors of Tyrosyl–DNA Phosphodiesterase I

Journal of medicinal chemistry, 2012-10, Vol.55 (20), p.8671-8684

2012

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DNA Containing Side Chains with Terminal Triple Bonds: Base-Pair Stability and Functionalization of Alkynylated Pyrimidines and 7-Deazapurines

Chemistry & biodiversity, 2006-05, Vol.3 (5), p.509-514

2006

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Modification of DNA with Octadiynyl Side Chains: Synthesis, Base Pairing, and Formation of Fluorescent Coumarin Dye Conjugates of Four Nucleobases by the Alkyne−Azide “Click” Reaction

Bioconjugate chemistry, 2008-01, Vol.19 (1), p.211-224

2008

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Nucleosides and oligonucleotides containing 1,2,3-triazole residues with nucleobase tethers: Synthesis via the azide-alkyne ‘click’ reaction

Bioorganic & medicinal chemistry, 2008-09, Vol.16 (18), p.8427-8439

2008

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Pyrrolo-dC oligonucleotides bearing alkynyl side chains with terminal triple bonds: synthesis, base pairing and fluorescent dye conjugates prepared by the azide-alkyne "click" reaction

Organic & biomolecular chemistry, 2008-01, Vol.6 (9), p.1674-1687

2008

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Clicking 3′-Azidothymidine into Novel Potent Inhibitors of Human Immunodeficiency Virus

Journal of medicinal chemistry, 2013-11, Vol.56 (21), p.8765-8780

2013

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1,N6-Etheno-2′-deoxytubercidin and pyrrolo-C: synthesis, base pairing, and fluorescence properties of 7-deazapurine nucleosides and oligonucleotides

Tetrahedron, 2007-04, Vol.63 (17), p.3471-3482

2007

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DNA with Branched Internal Side Chains: Synthesis of 5-Tripropargylamine-dU and Conjugation by an Azide-Alkyne Double Click Reaction

Chembiochem : a European journal of chemical biology, 2008-09, Vol.9 (14), p.2305-2316

2008

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7-Deazapurine and 8-Aza-7-deazapurine Nucleoside and Oligonucleotide Pyrene “Click” Conjugates: Synthesis, Nucleobase Controlled Fluorescence Quenching, and Duplex Stability

Journal of organic chemistry, 2012-01, Vol.77 (1), p.188-199

2012

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3-bromo-1-(2-deoxy-β-d-erythropentofuranosyl)-1- H-pyrazolo[3,4-d]-pyrimidine-4,6-diamine: a nucleoside which strongly enhances DNA duplex stability

Acta crystallographica. Section C, Crystal structure communications, 2005-02, Vol.61 (2), p.o67-o69

2005

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1, N 6-Etheno-2′-deoxytubercidin and pyrrolo-C: synthesis, base pairing, and fluorescence properties of 7-deazapurine nucleosides and oligonucleotides

Tetrahedron, 2007-04, Vol.63 (17), p.3471-3482

2007

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Nucleosides And Oligonucleotides With Diynyl Side Chains: The Huisgen-Sharpless Cycloaddition "Click Reaction" Performed On Dna And Their Constituents

Nucleosides, nucleotides & nucleic acids, 2007-01, Vol.26 (6-7), p.597-601

2007

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MPX-004 and MPX-007: New Pharmacological Tools to Study the Physiology of NMDA Receptors Containing the GluN2A Subunit: e0148129

PloS one, 2016-02, Vol.11 (2)

2016

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Corrigendum to “1, N6-etheno-2′-deoxytubercidin and pyrrolo-C: synthesis, base pairing, and fluorescence properties of 7-deazapurine nucleosides and oligonucleotides” : [Tetrahedron 63 (2007) 3471–3482]

Tetrahedron, 2007-09, Vol.63 (38), p.9567-9567

2007

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3-Bromo-1-(2-deoxy-β-d-erythro-pentofuranosyl)-1H-pyrazolo[3,4-d]pyrimidine-4,6-diamine: a nucleoside which strongly enhances DNA duplex stability

Acta crystallographica. Section C, Crystal structure communications, 2005-02, Vol.61 (2), p.o67-o69

2005

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3-Bromo-1-(2-deoxy-beta-D-erythro-pentofuranosyl)-1H-pyrazolo[3,4-d]pyrimidine-4,6-diamine: a nucleoside which strongly enhances DNA duplex stability

Acta crystallographica. Section C, Crystal structure communications, 2005-02, Vol.61 (Pt 2), p.o67-o69

2005

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ChemInform Abstract: Nucleosides and Oligonucleotides with Diynyl Side Chains: The Huisgen-Sharpless Cycloaddition "Click Reaction" Performed on DNA and Their Constituents

ChemInform, 2008-03, Vol.39 (10), p.no-no

2008

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3-Bromo-1-(2-deoxy-β-D-erythro-pentofuranosyl)-1H-pyrazolo [3,4-d]pyrimidine-4,6-diamine: A Nucleoside which Strongly Enhances DNA Duplex Stability

ChemInform, 2005-06, Vol.36 (26), p.no-no

2005

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1,N 6 ‐Etheno‐2′‐doexytubercidin and Pyrrolo‐C: Synthesis, Base Pairing, and Fluorescence Properties of 7‐Deazapurine Nucleosides and Oligonucleotides

ChemInform, 2007-06, Vol.38 (26)

2007

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1,N6-Etheno-2′-doexytubercidin and Pyrrolo-C: Synthesis, Base Pairing, and Fluorescence Properties of 7-Deazapurine Nucleosides and Oligonucleotides

ChemInform, 2007-06, Vol.38 (26), p.no-no

2007

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Nucleosides and Oligonucleotides with Diynyl Side Chains: Base Pairing and Functionalization of 2′-Deoxyuridine Derivatives by the Copper(I)-Catalyzed AlkyneAzide 'Click' Cycloaddition

MPX-004 and MPX-007: New Pharmacological Tools to Study the Physiology of NMDA Receptors Containing the GluN2A Subunit

5‑Arylidenethioxothiazolidinones as Inhibitors of Tyrosyl–DNA Phosphodiesterase I

DNA Containing Side Chains with Terminal Triple Bonds: Base-Pair Stability and Functionalization of Alkynylated Pyrimidines and 7-Deazapurines

Modification of DNA with Octadiynyl Side Chains: Synthesis, Base Pairing, and Formation of Fluorescent Coumarin Dye Conjugates of Four Nucleobases by the Alkyne−Azide “Click” Reaction

Nucleosides and oligonucleotides containing 1,2,3-triazole residues with nucleobase tethers: Synthesis via the azide-alkyne ‘click’ reaction

Pyrrolo-dC oligonucleotides bearing alkynyl side chains with terminal triple bonds: synthesis, base pairing and fluorescent dye conjugates prepared by the azide-alkyne "click" reaction

Clicking 3′-Azidothymidine into Novel Potent Inhibitors of Human Immunodeficiency Virus

1,N6-Etheno-2′-deoxytubercidin and pyrrolo-C: synthesis, base pairing, and fluorescence properties of 7-deazapurine nucleosides and oligonucleotides

DNA with Branched Internal Side Chains: Synthesis of 5-Tripropargylamine-dU and Conjugation by an Azide-Alkyne Double Click Reaction

7-Deazapurine and 8-Aza-7-deazapurine Nucleoside and Oligonucleotide Pyrene “Click” Conjugates: Synthesis, Nucleobase Controlled Fluorescence Quenching, and Duplex Stability

3-bromo-1-(2-deoxy-β-d-erythropentofuranosyl)-1- H-pyrazolo[3,4-d]-pyrimidine-4,6-diamine: a nucleoside which strongly enhances DNA duplex stability

1, N 6-Etheno-2′-deoxytubercidin and pyrrolo-C: synthesis, base pairing, and fluorescence properties of 7-deazapurine nucleosides and oligonucleotides

Nucleosides And Oligonucleotides With Diynyl Side Chains: The Huisgen-Sharpless Cycloaddition "Click Reaction" Performed On Dna And Their Constituents

MPX-004 and MPX-007: New Pharmacological Tools to Study the Physiology of NMDA Receptors Containing the GluN2A Subunit: e0148129

Corrigendum to “1, N6-etheno-2′-deoxytubercidin and pyrrolo-C: synthesis, base pairing, and fluorescence properties of 7-deazapurine nucleosides and oligonucleotides” : [Tetrahedron 63 (2007) 3471–3482]

3-Bromo-1-(2-deoxy-β-d-erythro-pentofuranosyl)-1H-pyrazolo[3,4-d]pyrimidine-4,6-diamine: a nucleoside which strongly enhances DNA duplex stability

3-Bromo-1-(2-deoxy-beta-D-erythro-pentofuranosyl)-1H-pyrazolo[3,4-d]pyrimidine-4,6-diamine: a nucleoside which strongly enhances DNA duplex stability

ChemInform Abstract: Nucleosides and Oligonucleotides with Diynyl Side Chains: The Huisgen-Sharpless Cycloaddition "Click Reaction" Performed on DNA and Their Constituents

3-Bromo-1-(2-deoxy-β-D-erythro-pentofuranosyl)-1H-pyrazolo [3,4-d]pyrimidine-4,6-diamine: A Nucleoside which Strongly Enhances DNA Duplex Stability

1,N 6 ‐Etheno‐2′‐doexytubercidin and Pyrrolo‐C: Synthesis, Base Pairing, and Fluorescence Properties of 7‐Deazapurine Nucleosides and Oligonucleotides

1,N6-Etheno-2′-doexytubercidin and Pyrrolo-C: Synthesis, Base Pairing, and Fluorescence Properties of 7-Deazapurine Nucleosides and Oligonucleotides

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