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Synthesis of 2′-deoxy-2′-fluoro-2′-C-methyl spiro cyclopentyl carbocyclic uridine analog as potential inhibitors of HCV NS5B polymerase

Nucleosides, nucleotides & nucleic acids, 2020-02, Vol.39 (1-3), p.52-68

2020

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A Convergent Approach for the Synthesis of Ara-Neplanocin a Analogues Under Subzero Microwave Assisted Conditions

Nucleosides, nucleotides & nucleic acids, 2009-05, Vol.28 (5-7), p.504-518

2009

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Synthesis and Anti-HIV Activity of β-D-3′-Azido-2′,3′-unsaturated Nucleosides and β-D-3′-Azido-3′-deoxyribofuranosylnucleosides

Nucleosides, nucleotides & nucleic acids, 2005-01, Vol.24 (10-12), p.1707-1727

2005

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2′-Fluoro-4′-thio-2′,3′-unsaturated Nucleosides: Anti-HIV Activity, Resistance Profile, and Molecular Modeling Studies

Nucleosides, nucleotides & nucleic acids, 2003-10, Vol.22 (5-8), p.611-615

2003

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A Practical Synthesis of L-FMAU from L-Arabinose

Nucleosides & nucleotides, 1999-02, Vol.18 (2), p.187-195

1999

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Acetylation of Nucleosides by Acetylsalicylic Acid (Aspirin)1

Nucleosides & nucleotides, 1983-01, Vol.2 (5), p.453-458, Article 453

Chu, Chung K.

1983

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SYNTHESIS AND IN VITRO ANTI-HCV ACTIVITY OF β-D- and L-2′-DEOXY-2′-FLUORORIBONUCLEOSIDES

Nucleosides, nucleotides & nucleic acids, 2005-04, Vol.24 (5-7), p.875-879

2005

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SYNTHESIS OF CARBOCYCLIC OROTIDINE ANALOGS AS POTENTIAL OROTIDINE DECARBOXYLASE INHIBITORS

Nucleosides, nucleotides & nucleic acids, 2001-12, Vol.20 (12), p.1915-1925

2001

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New Classes of Fluorinated L-Nucleosides; Synthesis and Antiviral Activity

Nucleosides & nucleotides, 1999-04, Vol.18 (4-5), p.537-540

1999

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Synthesis and in vitro anti-HCV activity of beta-D- and 1-2'-deoxy-2'-fluororibonucleosides

Nucleosides, nucleotides & nucleic acids, 2005, Vol.24 (5-7), p.875

2005

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UNDERSTANDING THE MODE OF ACTION OF L-NUCLEOSIDES AS ANTIVIRAL AGENTS: A MOLECULAR MODELING APPROACH

Nucleosides, nucleotides & nucleic acids, 2001-04, Vol.20 (4-7), p.385-388

2001

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Asymmetric Synthesis of Oxazolidine Nucleosides and Related Chemistry

Nucleosides & nucleotides, 1998-01, Vol.17 (1-3), p.1-13

1998

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Synthesis of L-3′-Hydroxymethylribonucleosides

Nucleosides, nucleotides & nucleic acids, 2000-01, Vol.19 (1-2), p.219-236

2000

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Synthesis and Antiviral Activities of Enantiomeric 1-[2-(Hydroxymethyl) Cyclopropyl] Methyl Nucleosides

Nucleosides, nucleotides & nucleic acids, 2000-01, Vol.19 (1-2), p.253-268

2000

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Stereoselective Synthesis of 2′,3′-Dideoxy-and 2,3′-Didehydro-2′,3′-dideoxy-nucleosides

Nucleosides & nucleotides, 1991-01, Vol.10 (1-3), p.423-426

1991

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A Practical Synthesis of 2′-Deoxyuridine from Uridine

Synthetic communications, 1990-04, Vol.20 (7), p.1039-1046

1990

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A General Synthetic Method for 2′,3′-Dideoxynucleosldes: Total Synthetic Approach

Nucleosides & nucleotides, 1989-01, Vol.8 (5-6), p.903-906

1989

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Syntheses of 2″,3″-Dideoxy-L-Glycero-Pentofuranosyl C-Nucleosides

Nucleosides & nucleotides, 1996-06, Vol.15 (6), p.1223-1236

1996

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L-Nucleoside Analogues as Potential Antimalarials That Selectively Target Plasmodium Falclparum Adenosine Deaminase

Nucleosides & nucleotides, 1999-11, Vol.18 (11-12), p.2521-2532

1999

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L-Nucleoside Analogues as Potential Antimalarials That Selectively Target Plasmodium Falclparum Adenosine Deaminase

Nucleosides & nucleotides, 1999-11, Vol.18 (11-12), p.2521-2532

1999

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SYNTHESES OF 2′,3′-DIDEOXY-D-C-NUCLEOSIDES FROM γ-LACTONE

Nucleosides & nucleotides, 1996-11, Vol.15 (11-12), p.1821-1834

1996

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Synthesis of 2′-C-α-Methyl-2′,3′-dideoxynucleosides

Nucleosides & nucleotides, 1996-01, Vol.15 (1-3), p.183-204

1996

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L-Purine Nucleosides as Selective Antimalarials

Nucleosides & nucleotides, 1999-04, Vol.18 (4-5), p.885-889

1999

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Synthesis of 2′,3′-Dideoxy-2′-Fluoro-l-threo-Pentofuranosyl Nucleosides as Potential Antiviral Agents

Nucleosides & nucleotides, 1999-10, Vol.18 (10), p.2233-2252

1999

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Practical Synthesis of AZT and AZDU from Xylose: Efficient Deoxygenation via Nucleoside 2′-Xanthates

Nucleosides & nucleotides, 1992-02, Vol.11 (2-4), p.693-705

1992

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Synthesis of 2′-deoxy-2′-fluoro-2′-C-methyl spiro cyclopentyl carbocyclic uridine analog as potential inhibitors of HCV NS5B polymerase

A Convergent Approach for the Synthesis of Ara-Neplanocin a Analogues Under Subzero Microwave Assisted Conditions

Synthesis and Anti-HIV Activity of β-D-3′-Azido-2′,3′-unsaturated Nucleosides and β-D-3′-Azido-3′-deoxyribofuranosylnucleosides

2′-Fluoro-4′-thio-2′,3′-unsaturated Nucleosides: Anti-HIV Activity, Resistance Profile, and Molecular Modeling Studies

A Practical Synthesis of L-FMAU from L-Arabinose

Acetylation of Nucleosides by Acetylsalicylic Acid (Aspirin)1

SYNTHESIS AND IN VITRO ANTI-HCV ACTIVITY OF β-D- and L-2′-DEOXY-2′-FLUORORIBONUCLEOSIDES

SYNTHESIS OF CARBOCYCLIC OROTIDINE ANALOGS AS POTENTIAL OROTIDINE DECARBOXYLASE INHIBITORS

New Classes of Fluorinated L-Nucleosides; Synthesis and Antiviral Activity

Synthesis and in vitro anti-HCV activity of beta-D- and 1-2'-deoxy-2'-fluororibonucleosides

UNDERSTANDING THE MODE OF ACTION OF L-NUCLEOSIDES AS ANTIVIRAL AGENTS: A MOLECULAR MODELING APPROACH

Asymmetric Synthesis of Oxazolidine Nucleosides and Related Chemistry

Synthesis of L-3′-Hydroxymethylribonucleosides

Synthesis and Antiviral Activities of Enantiomeric 1-[2-(Hydroxymethyl) Cyclopropyl] Methyl Nucleosides

Stereoselective Synthesis of 2′,3′-Dideoxy-and 2,3′-Didehydro-2′,3′-dideoxy-nucleosides

A Practical Synthesis of 2′-Deoxyuridine from Uridine

A General Synthetic Method for 2′,3′-Dideoxynucleosldes: Total Synthetic Approach

Syntheses of 2″,3″-Dideoxy-L-Glycero-Pentofuranosyl C-Nucleosides

L-Nucleoside Analogues as Potential Antimalarials That Selectively Target Plasmodium Falclparum Adenosine Deaminase

L-Nucleoside Analogues as Potential Antimalarials That Selectively Target Plasmodium Falclparum Adenosine Deaminase

SYNTHESES OF 2′,3′-DIDEOXY-D-C-NUCLEOSIDES FROM γ-LACTONE

Synthesis of 2′-C-α-Methyl-2′,3′-dideoxynucleosides

L-Purine Nucleosides as Selective Antimalarials

Synthesis of 2′,3′-Dideoxy-2′-Fluoro-l-threo-Pentofuranosyl Nucleosides as Potential Antiviral Agents

Practical Synthesis of AZT and AZDU from Xylose: Efficient Deoxygenation via Nucleoside 2′-Xanthates

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