Nucleophilic N1 → N3 Rearrangement of 5′-O-Trityl-O2,3′-Cycloanhydrothymidine
Author:
Affiliation:
1. a Polish Academy of Sciences, Centre of Molecular and Macromolecular Studies , Sienkiewicza 112, 90-363 , łódź , Poland
2. b Technical University in łódź, Institute of General Food Chemistry , Stefanowskiego 4/10, 90-924 , łódź , Poland
Publisher
Informa UK Limited
Subject
Genetics,Molecular Medicine,Biochemistry,General Medicine
Link
https://www.tandfonline.com/doi/pdf/10.1080/15257770008045451
Reference40 articles.
1. Nucleosides. XVI. Further Studies of Anhydronucleosides1
2. Nucleosides. III. 1-(2'-Deoxy-3',5'-epoxy-β-D-threo-pentofuranosyl) thymine1,2
3. Wolfrom , M. L. and Tipson , R. S. 1969. Advances in Carbohydrate Chemistry and Biochemistry, 177–188. New York: Academic press.
4. Nucleotide synthesis. IV. Phosphorylated 3'-amino-3'-deoxythymidine and 5'-amino-5'-deoxythymidine and derivatives
5. A convenient procedure for formation of certain uracil and thymine anhydronucleosides
Cited by 3 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. ChemInform Abstract: Nucleophilic N1→N3 Rearrangement of 5′-O-Trityl-O2,3-cycloanhydrothymidine.;ChemInform;2010-05-21
2. Reactions of Transglycosylation in the Nucleoside Chemistry;Current Organic Chemistry;2008-03-01
3. Rearrangement Reactions of Guanosine Cyclonucleosides and Their Analogs;Nucleosides, Nucleotides and Nucleic Acids;2003-10
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