Synthesis and biological evaluation of inosine phosphonates
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Materials Chemistry,General Chemistry,Catalysis
Link
http://pubs.rsc.org/en/content/articlepdf/2010/NJ/B9NJ00574A
Reference18 articles.
1. Nucleosides. XV. Decarboxylative elimination of 2'-deoxynucleoside uronic acids
2. Regiospecific and highly stereoselective electrophilic addition to furanoid glycals: synthesis of phosphonate nucleotide analogs with potent activity against HIV
3. Synthesis, anti-HIV activity, and resistance profile of thymidine phosphonomethoxy nucleosides and their bis-isopropyloxymethylcarbonyl (bisPOC) prodrugs
4. Synthesis, anti-HIV activity, and resistance profiles of ribose modified nucleoside phosphonates
5. Utility of 1-(5’-Acetoxy-4’-Benzoyltetrahydrofuran-2’-yl)-3-Benzyloxymethylthymine for the Synthesis of 5’-Modified Furanoid Nucleoside Analogs1
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1. Synthesis of a 3′-Deoxy-C -Nucleoside Phosphonate Bearing 9-Deazaadenine as Base Moiety;European Journal of Organic Chemistry;2018-12-06
2. Synthesis of a C-Nucleoside Phosphonate by Base-Promoted Epimerization;Organic Letters;2018-02-01
3. Synthesis of a 3′-Fluoro-3′-deoxytetrose Adenine Phosphonate;The Journal of Organic Chemistry;2017-08-29
4. Stereoselective Biotransformations as an Effective Tool for the Synthesis of Chiral Compounds with P-C Bond – Scope and Limitations of the Methods;Current Organic Chemistry;2012-05-01
5. Alkynyl and Phosphonyl Substituted Nucleobases: A Case of Thermally Induced Conformational Polymorphism;Crystal Growth & Design;2011-05-03
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