Carbon-Carbon Bond Formation at the Sugar Portion of Nucleosides: Synthetic Potential of Unsaturated-sugar Nucleosides
Author:
Publisher
The Society of Synthetic Organic Chemistry, Japan
Subject
Organic Chemistry
Cited by 9 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. An alternative method for the synthesis of 2′-halogeno-1′,2′-unsaturated uridine derivatives through syn-elimination of pivalic acid of 2′-halogeno- 2′-deoxy-1′-pivaloyloxyuracil nucleoside: preparation of its 2′-C-branched nucleosides;Nucleosides, Nucleotides & Nucleic Acids;2019-08-20
2. Synthesis of 3′,4′-difluoro-3′-deoxyribonucleosides and its evaluation of the biological activities: Discovery of a novel type of anti-HCV agent 3′,4′-difluorocordycepin;Bioorganic & Medicinal Chemistry;2014-11
3. Synthesis of novel 4′-C-methyl-1′,3′-dioxolane pyrimidine nucleosides and evaluation of its anti-HIV-1 activity;Tetrahedron;2013-12
4. Phenylsulfanylation of 3′,4′-Unsaturated Adenosine Employing Thiophenol-N-Iodosuccinimide Leads to 4′-Phenylsulfanylcordycepin: Synthesis of 4′-Substituted Cordycepins on the Basis of Substitution of the Phenylsulfanyl Leaving Group;The Journal of Organic Chemistry;2011-10-06
5. Synthesis and anti-HIV-1 evaluation of phosphonates which mimic the 5′-monophosphate of 4′-branched 2′,3′-didehydro-2′,3′-dideoxy nucleosides;Bioorganic & Medicinal Chemistry;2010-10-15
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