A practical synthetic route to 4′-alkylaristeromycin derivatives: 4′-methylaristeromycin
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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3. A Convenient Asymmetric Synthesis of 4‘-α-Carboxylated Nucleosides
4. Asymmetric Synthesis of C4‘α-Carboxylated 2‘-Deoxynucleosides. Preparation of Oxetanone Derivatives and Influence of Solvent on the Stereochemistry of Base Introduction
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1. Synthesis and Antiviral Evaluation of Carbocyclic Nucleoside Analogs of Nucleoside Reverse Transcriptase Translocation Inhibitor MK-8591 (4′-Ethynyl-2-fluoro-2′-deoxyadenosine);Journal of Medicinal Chemistry;2018-09-28
2. A review of methods to synthesise 4′-substituted nucleosides;Org. Biomol. Chem.;2014
3. 6′-Methyl-5′-homoaristeromycin: A structural variation of the anti-orthopox virus candidate 5′-homoaristeromycin;Bioorganic & Medicinal Chemistry;2013-07
4. 2-Azabicyclo[2.2.1]hept-5-en-3-one: Chemical Profile of a Versatile Synthetic Building Block and its Impact on the Development of Therapeutics;Chemical Reviews;2012-06-08
5. Stereocontrolled Synthesis and Biological Evaluation of Novel Carbocyclic Nucleosides Analogues of Neplanocin F and Abacavir;Synlett;2010-12-10
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