Synthesis of 6,6′-(S)-cyclo-2′-deoxyuridine featuring a unique Barbier-style cyclization
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemical Engineering,General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2012/RA/C2RA21559D
Reference22 articles.
1. Synthesis and Properties of DNA Containing Cyclonucleosides
2. An efficient synthetic approach to 6,5′-(S)- and 6,5′-(R)-cyclouridine
3. Nucleosides. 101. Conformationally restricted analogs of pyrimidine nucleosides. 1. Synthesis of 6,5'(S)- and 6,5'(R)-cyclouridine
4. Black Light Induced Radical Cyclization Approach to Cyclonucleosides: An Independent Approach
5. (Nucleosides and nucleotides. LXXIII). Synthesis of 6,5'-cyclo-5'-deoxy-5'(R and S)-(2-hydroxyethyl)-uridines.
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1. Constrained nucleoside analogues – Crystal and molecular structure of 6,5′-O-anhydrouridines fixed in the anti conformation;Journal of Molecular Structure;2015-10
2. Addition of Vinylmetallic Reagents to Chiral 2-Formyltetrahydrofuran;European Journal of Organic Chemistry;2014-11-17
3. The synthesis and structural characterization of both diastereomers of 5′-(hydroxymethyl)-6,5′-cyclo-2′,5′-dideoxyuridine cyclonucleosides;RSC Advances;2014-07-01
4. Synthesis and NMR Assignment of the Two Diastereomers of 8,6′-Cyclo-2′,6′-Dideoxyadenosine;Nucleosides, Nucleotides and Nucleic Acids;2013-01
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