Regioselective 2′-O-debenzoylation of 2',3'-di-O-benzoyl threose nucleosides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Chemical Etiology of Nucleic Acid Structure: The α-Threofuranosyl-(3'→2') Oligonucleotide System
2. The -L-Threofuranosyl-(3′→2′)-oligonucleotide System (‘TNA'): Synthesis and Pairing Properties
3. Crystal Structure of a B-Form DNA Duplex Containing (l)-α-Threofuranosyl (3‘→2‘) Nucleosides: A Four-Carbon Sugar Is Easily Accommodated into the Backbone of DNA
4. Why Does TNA Cross-Pair More Strongly with RNA Than with DNA? An Answer From X-ray Analysis
5. Base-Pairing Systems Related to TNA: α-Threofuranosyl Oligonucleotides Containing Phosphoramidate Linkages1
Cited by 4 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. Scalable Synthesis, In Vitro cccDNA Reduction, and In Vivo Antihepatitis B Virus Activity of a Phosphonomethoxydeoxythreosyl Adenine Prodrug;Journal of Medicinal Chemistry;2020-11-16
2. Synthesis of a Threosyl-C-nucleoside Phosphonate;European Journal of Organic Chemistry;2019-10-14
3. A Scalable Synthesis of α-l-Threose Nucleic Acid Monomers;The Journal of Organic Chemistry;2016-02-26
4. ChemInform Abstract: Regioselective 2′-O-Debenzoylation of 2′,3′-Di-O-benzoyl Threose Nucleosides.;ChemInform;2014-02-27
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