Nucleophilic substitution approach to 4′-substituted thymidines by employing 4′-benzenesulfonyl leaving group
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference19 articles.
1. Potential of 4′-C-Substituted Nucleosides for the Treatment of HIV-1
2. Nucleosides and Nucleotides. 185. Synthesis and Biological Activities of 4‘α-C-Branched-Chain Sugar Pyrimidine Nucleosides
3. Syntheses of 4‘-C-Ethynyl-β-d-arabino- and 4‘-C-Ethynyl-2‘-deoxy-β-d-ribo-pentofuranosylpyrimidines and -purines and Evaluation of Their Anti-HIV Activity
4. Ring Opening of 4‘,5‘-Epoxynucleosides: A Novel Stereoselective Entry to 4‘-C-Branched Nucleosides
5. Synthesis of a highly active new anti-HIV agent 2′,3′-Didehydro-3′-deoxy-4′-ethynylthymidine
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