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
Author:
Affiliation:
1. Department of Pharmaceutical Sciences, Nihon Pharmaceutical University, Saitama, Japan;
2. School of Pharmacy, Showa University, Tokyo, Japan
Publisher
Informa UK Limited
Subject
Genetics,Molecular Medicine,Biochemistry,General Medicine
Link
https://www.tandfonline.com/doi/pdf/10.1080/15257770.2019.1641724
Reference29 articles.
1. AIDS-driven nucleoside chemistry.
2. Nucleosides and Nucleotides as Antitumor and Antiviral Agents
3. ChemInform Abstract: Nucleoside and Non-nucleoside IMP Dehydrogenase Inhibitors as Antitumor and Antiviral Agents
4. Sugar-Modified Nucleosides in Past 10 Years, A Review
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