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Collect. Czech. Chem. Commun. 2010, 75, 33-57
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. <>
  • 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. <>
  • Sobkowski Michal: ChemInform Abstract: A Convenient Protection for 4‐Oxopyrimidine Moieties in Nucleosides by the Pivaloyl Group. ChemInform 2010, 41. <>
  • Sobkowski Michal: Chemistry and stereochemistry of internucleotide bond formation by the H-phosphonate method. New J. Chem. 2010, 34, 854. <>
  • 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. <>