Efficient Synthesis of 2‘-C-β-Methylguanosine
Author:
Affiliation:
1. Howard Hughes Medical Institute, Department of Biochemistry & Molecular Biology and Department of Chemistry, The University of Chicago, 5841 South Maryland Avenue, MC 1028, Chicago, Illinois 60637 nli@uchicago.edu; jpicciri@uchicago.edu
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo0602165
Reference20 articles.
1. A Short, Flexible Route toward 2‘-C-Branched Ribonucleosides
2. Structure−Activity Relationship of Purine Ribonucleosides for Inhibition of Hepatitis C Virus RNA-Dependent RNA Polymerase
3. Structure−Activity Relationship of Heterobase-Modified 2‘-C-Methyl Ribonucleosides as Inhibitors of Hepatitis C Virus RNA Replication
4. New Strategies for Exploring RNA's 2′-OH Expose the Importance of Solvent during Group II Intron Catalysis
5. Synthesis of the Phosphoramidite Derivative of 2‘-Deoxy-2‘-C-β-methylcytidine
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3. In Vitro and In Vivo Characterization of the Anti-Zika Virus Activity of ProTides of 2′-C-β-Methylguanosine;ACS Infectious Diseases;2020-06-11
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