New synthesis of 3′--substituted-3′-nitromethyl-ribo-thymidines
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference62 articles.
1. A cyclic voltammetric study of the -chlorination of zinc octaethylporphyrin via anodic oxidation
2. Michael addition reactions of α β-ene-3′-phenylselenone of uridine. New synthesis of 2′,3′-dideoxy-ribo-aziridino-, 2′,3′-dideoxy-2′, 3′-ribo-cyclopropyl- & 2,2′-O-anhydro-3′-deoxy-3′-amino uridine derivatives
3. New synthesis of 2',3'-dideoxy-3'-C-cyano-2'-substituted thymidines by michael addition reactions
4. New syntheses of 2',3'-dideoxy-2',3'-di-substituted & -2'-mono-substituted uridines & adenosines by michael addition reactions
5. Synthesis of 2′,3′-Dideoxy-3′-nitro-2′,3′-didehydrothymidine. Its Use as a General Intermediate for the Preparation of Various 2′,3′-Substituted Nucleosides
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1. Growing the Molecular Architecture at Alkynyl(amino)carbene Ligands in Diiron µ‐Aminocarbyne Complexes;European Journal of Inorganic Chemistry;2016-09-13
2. ChemInform Abstract: New Synthesis of 3′-C-Substituted-3′-nitromethyl-ribo-thymidines.;ChemInform;2010-08-19
3. N−C Bond Formation of NO Ligands on Ruthenium Complexes with Concurrent Vinylic C−H Activation and Subsequent Proton-Induced Reactivities of the Resulting Nitrosovinyl Species;Journal of the American Chemical Society;2008-07-18
4. Fine Synthetic Nucleoside Chemistry Based on Nucleoside Natural Products Synthesis;Chemical and Pharmaceutical Bulletin;2008
5. A simple and stereodivergent strategy for the synthesis of 3′-C-branched 2′,3′-dideoxynucleosides exploiting (Z)-but-2-en-1,4-diol and (R)-2,3-cyclohexylideneglyceraldehyde;Tetrahedron Letters;2006-07
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