The synthesis and structural characterization of both diastereomers of 5′-(hydroxymethyl)-6,5′-cyclo-2′,5′-dideoxyuridine cyclonucleosides
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemical Engineering,General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2014/RA/C4RA04784B
Reference20 articles.
1. Synthesis and reactions of spirooxiranes in the 6,5'-cyclopyrimidine nucleoside series: preparation of 5'-deoxy-5'-(hydroxymethyl)-6,5'(S)- and -6,5'(R)-cyclouridines
2. Nucleosides. 101. Conformationally restricted analogs of pyrimidine nucleosides. 1. Synthesis of 6,5'(S)- and 6,5'(R)-cyclouridine
3. Nucleosides and nucleotides. LXXII Synthesis of 6,5'-cyclo-2',5'-dideoxypyrimidine nucleosides.
4. The synthesis of 6,6′-cyclo-6′-deoxyhexofuranosyluracilsviaa diazomethane-promoted ring-enlargement reaction
5. Synthesis of 6,5'-cyclo-5'-deoxyuridines by radical cyclization (nucleosides and nucleotides. L).
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1. Synthesis and applications of cyclonucleosides: an update (2010–2023);Molecular Diversity;2023-10-27
2. Bicyclic 6-6 Systems With One Bridgehead (Ring Junction) Nitrogen Atom: Two Extra Heteroatoms 1:1;Comprehensive Heterocyclic Chemistry IV;2022
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