Collect. Czech. Chem. Commun.
2010, 75, 33-57
https://doi.org/10.1135/cccc2009084
Published online 2010-02-08 13:36:33
A convenient protection for 4-oxopyrimidine moieties in nucleosides by the pivaloyl group
Michał Sobkowski
Institute of Bioorganic Chemistry, Polish Academy of Sciences, Noskowskiego 12/14, 61-704 Poznań, Poland
Crossref Cited-by Linking
- Eyberg Juri, Göhringer Daniela, Salihovic Amila, Richert Clemens: Acid‐Stable Nucleobase Protection for a Strongly Pairing Pyridone C‐Nucleoside Suitable for Solid‐Phase Synthesis of Oligonucleotides. Eur J Org Chem 2022, 2022. <https://doi.org/10.1002/ejoc.202200611>
- Bartosik Karolina, Sochacka Elzbieta, Leszczynska Grazyna: Post-synthetic conversion of 5-pivaloyloxymethyluridine present in a support-bound RNA oligomer into biologically relevant derivatives of 5-methyluridine. Org. Biomol. Chem. 2017, 15, 2097. <https://doi.org/10.1039/C6OB02674E>
- Sobkowski Michal: ChemInform Abstract: A Convenient Protection for 4‐Oxopyrimidine Moieties in Nucleosides by the Pivaloyl Group. ChemInform 2010, 41. <https://doi.org/10.1002/chin.201029208>
- Sobkowski Michal: Chemistry and stereochemistry of internucleotide bond formation by the H-phosphonate method. New J. Chem. 2010, 34, 854. <https://doi.org/10.1039/b9nj00679f>
- Sobkowski Michal, Stawinski Jacek, Kraszewski Adam: Stereochemistry of Internucleotide Bond Formation by the H-Phosphonate Method. 5. The Role of Brønsted and H-Bonding Base Catalysis in Ribonucleoside H-Phosphonate Condensation—Chemical and Stereochemical Consequences. Nucleos Nucleot Nuc Acids 2010, 29, 628. <https://doi.org/10.1080/15257770.2010.497014>
