Synthesis of pyrrolidin-1-yl analogues of pyrimidine dideoxynucleosides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. Inhibition of the in vitro infectivity and cytopathic effect of human T-lymphotrophic virus type III/lymphadenopathy-associated virus (HTLV-III/LAV) by 2',3'-dideoxynucleosides.
2. Comparative activity of 2′,3′-saturated and unsaturated pyrimidine and purine nucleosides against human immunodeficiency virus type 1 in peripheral blood mononuclear cells
3. In Vivo Activity Against HIV and Favorable Toxicity Profile of 2′,3′-Dideoxyinosine
4. Potent and selective activity of a new carbocyclic nucleoside analog (Carbovir: NSC 614846) against human immunodeficiency virus In vitro
5. Synthesis of iso-ddA, member of a novel class of anti-HIV agents
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1. Synthesis, conformational studies, and biological properties of phosphonomethoxyethyl derivatives of nucleobases with a locked conformation via a pyrrolidine ring;Organic & Biomolecular Chemistry;2015
2. Nucleoside Analogues: Synthesis and Biological Properties of Azanucleoside Derivatives;European Journal of Organic Chemistry;2014-02-20
3. ChemInform Abstract: Synthesis of Pyrrolidin-1-yl Analogues of Pyrimidine Dideoxynucleosides.;ChemInform;2010-08-22
4. Pyrrolidine N-alkylphosphonates and related nucleotide analogues: synthesis and stereochemistry;Tetrahedron;2009-05
5. Synthesis and antiviral properties of aza-analogues of ganciclovir derived from 5,5-bis(hydroxymethyl)pyrrolidin-2-one;Tetrahedron;2007-10
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