Construction of Pyrimidine Bases Bearing Carboxylic Acid Equivalents at the C5 Position by Postsynthetic Modification of Oligonucleotides
Author:
Affiliation:
1. Faculty of Pharmaceutical SciencesTokushima Bunri University Nishihama, Yamashiro‐cho Tokushima Japan
Funder
Japan Society for the Promotion of Science
Publisher
Wiley
Subject
General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/cpnc.91
Reference25 articles.
1. Oligonucleotide based artificial nuclease (OBAN) systems. Bulge size dependence and positioning of catalytic group in cleavage of RNA-bulges
2. Post-synthetic conversion of 5-pivaloyloxymethyluridine present in a support-bound RNA oligomer into biologically relevant derivatives of 5-methyluridine
3. Vinylsulfonamide and Acrylamide Modification of DNA for Cross-linking with Proteins
4. Modification of oligodeoxynucleotides by on-column Suzuki cross-coupling reactions
5. Nucleosides and Nucleotides. 160. Synthesis of Oligodeoxyribonucleotides Containing 5-(N-Aminoalkyl)carbamoyl-2‘-deoxyuridines by a New Postsynthetic Modification Method and Their Thermal Stability and Nuclease-Resistance Properties
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