Search Results - "Sari, Ozkan"
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Synthesis and antiviral evaluation of 2′,2′,3′,3′-tetrafluoro nucleoside analogs
Published in Tetrahedron letters (15-02-2017)“…[Display omitted] •The synthesis of novel 2′,2′,3′,3′-tetrafluoro nucleoside analogs is described.•Glycosylation reactions are achieved via Mitsunobu…”
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The Preparation of Trisubstituted Alkenyl Nucleoside Phosphonates under Ultrasound-Assisted Olefin Cross-Metathesis
Published in Organic letters (06-09-2013)“…Intermolecular ultrasound-assisted olefin cross-metathesis is reported. This approach allows an easy access to challenging trisubstituted alkenyl nucleoside…”
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Diastereoselective Synthesis of 2′-Dihalopyrimidine Ribonucleoside Inhibitors of Hepatitis C Virus Replication
Published in ACS omega (11-01-2022)“…We present a newly developed synthetic route to 2-bromo-2-fluoro ribolactone based on our published 2-chloro-2-fluoro ribolactone synthesis. Stereoselective…”
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Novel Hepatitis B Virus Capsid Assembly Modulator Induces Potent Antiviral Responses In Vitro and in Humanized Mice
Published in Antimicrobial agents and chemotherapy (27-01-2020)“…Hepatitis B virus (HBV) affects an estimated 250 million chronic carriers worldwide. Though several vaccines exist, they are ineffective for those already…”
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Synthesis of sulfamoylbenzamide derivatives as HBV capsid assembly effector
Published in European journal of medicinal chemistry (29-09-2017)“…The synthesis of novel series of sulfamoylbenzamides as HBV capsid assembly effector is reported. The structure was divided into five parts which were…”
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Discovery and structure activity relationship of glyoxamide derivatives as anti-hepatitis B virus agents
Published in Bioorganic & medicinal chemistry (01-02-2021)“…[Display omitted] Chronic hepatitis B viral infection is a significant health problem world-wide, and currently available antiviral agents suppress HBV…”
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Synthesis of (2S)‑2-Chloro-2-fluororibolactone via Stereoselective Electrophilic Fluorination
Published in Journal of organic chemistry (15-12-2017)“…A novel and efficient route for the preparation of (2S)-2-chloro-2-fluorolactone 29 is described. This approach takes advantage of a highly efficient…”
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2′-Chloro,2′-fluoro Ribonucleotide Prodrugs with Potent Pan-genotypic Activity against Hepatitis C Virus Replication in Culture
Published in Journal of medicinal chemistry (13-07-2017)“…Pan-genotypic nucleoside HCV inhibitors display a high genetic barrier to drug resistance and are the preferred direct-acting agents to achieve complete…”
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Synthesis of dihydropyrimidine α,γ-diketobutanoic acid derivatives targeting HIV integrase
Published in European journal of medicinal chemistry (02-11-2015)“…The synthesis and antiviral evaluation of a series of dihydropyrimidinone and thiopyrimidine derivatives bearing aryl α,γ-diketobutanoic acid moiety are…”
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Discovery of a Series of 2′-α-Fluoro,2′-β-bromo-ribonucleosides and Their Phosphoramidate Prodrugs as Potent Pan-Genotypic Inhibitors of Hepatitis C Virus
Published in Journal of medicinal chemistry (28-02-2019)“…Hepatitis C virus (HCV) nucleoside inhibitors display pan-genotypic activity, a high barrier to the selection of resistant virus, and are some of the most…”
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Synthesis and antiviral evaluation of C5-substituted-(1,3-diyne)-2′-deoxyuridines
Published in European journal of medicinal chemistry (01-07-2012)“…Starting from acetylated 5-ethynyl-2′-deoxyuridine (3), 14 hitherto unknown C5-substituted-(1,3-diyne)-2′-deoxyuridines (with cyclopropyl, hydroxymethyl,…”
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Synthesis and antiviral evaluation of bis(POM) prodrugs of (E)-[4′-phosphono-but-2′-en-1′-yl]purine nucleosides
Published in European journal of medicinal chemistry (01-11-2012)“…Seventeen hitherto unknown bis(POM) prodrugs of novel (E)-[4′-phosphono-but-2′-en-1′-yl]purine nucleosides were prepared in a straight approach and at good…”
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Sonication‐Assisted Synthesis of (E)‐2‐Methyl‐but‐2‐enyl Nucleoside Phosphonate Prodrugs
Published in ChemistrySelect (Weinheim) (01-08-2016)“…Several hitherto unknown acyclic 2‐methyl‐but‐2‐enyl nucleoside phosphonate analogs (ANPs) and their bis‐(pivaloyloxymethyl) prodrug forms were prepared by a…”
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