Synthesis of 1,3-oxathiolane derivatives as novel precursors of 2′,3′-dideoxy-3′-oxa-4′-thioribonucleosides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference9 articles.
1. Synthesis of enantiomerically pure (2'R,5'S)-(-)-1-(2-hydroxymethyloxathiolan-5-yl)cytosine as a potent antiviral agent against hepatitis B virus (HBV) and human immunodeficiency virus (HIV)
2. (±)-Dioxolane-T ((±)-1-[(2β,4β)-2-(hydroxymethyl)-4-dioxolanyl]thymine)
3. Asymmetric synthesis of 1,3-dioxolane-pyrimidine nucleosides and their anti-HIV activity.
4. A novel class of 1,3-oxathiolane nucleoside analogues having potent anti-HIV activity
5. Synthesis of optically active 2′,3′-dideoxy-3′-oxa-4′-thio-ribonucleoside analogues by transposition of a leaving group on chiral oxathiolanes via a reductive-oxidative process
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1. Silica gel-promoted new one-pot procedure for the synthesis of 1,3-oxathiolan-5-one;Journal of Sulfur Chemistry;2017-04-12
2. Vistas in the field of 1,3-oxathiolan-5-ones: Synthesis and chemical reactivity;Synthetic Communications;2016-11-18
3. A facile catalyst and solvent-free synthesis of spiro thia heterocycles on grinding;Journal of the Serbian Chemical Society;2011
4. ChemInform Abstract: Synthesis of 1,3-Oxathiolane Derivatives as Novel Precursors of 2′,3′- Dideoxy-3′-oxa-4′-thioribonucleosides.;ChemInform;2010-08-16
5. Ultrasound promoted greener synthesis of spiro[indole-3,5′-[1,3]oxathiolanes in water;Ultrasonics Sonochemistry;2010-02
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