An acetal group suitable for the protection of 2′-hydroxy functions in rapid oligoribonucleotide synthesis
- 1 January 1986
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 27 (20) , 2291-2294
- https://doi.org/10.1016/s0040-4039(00)84511-6
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Some Aspects of the Chemical Synthesis of OligoribonucleotidesNucleosides and Nucleotides, 1985
- Action of acid on oligoribonucleotide phosphotriester intermediates. Effect of released vicinal hydroxy functionsNucleic Acids Research, 1985
- The protection of 2′-hydroxy functions in oligoribonucleotide synthesisTetrahedron Letters, 1984
- Synthesis of the 3'-terminal decaribonucleoside nonaphosphate of yeast alanine transfer ribonucleic acidTetrahedron, 1980
- 4-methoxytetrahydropyran-4-ylTetrahedron, 1970
- The Synthesis of oligoribonucleotides—IVTetrahedron, 1968
- Symmetrical alternative to the tetrahydropyranyl protecting groupJournal of the American Chemical Society, 1967
- The synthesis of oligoribonucleotides—IIITetrahedron, 1967
- 985. The structure and properties of certain polycyclic indolo- and quinolino-derivatives. Part XV. Derivatives of 1-phenyl-4-piperidone and its phosphorus and arsenic analoguesJournal of the Chemical Society, 1962
- The Evaluation of Inductive and Resonance Effects on Reactivity. I. Hydrolysis Rates of Acetals of Non-conjugated Aldehydes and Ketones1aJournal of the American Chemical Society, 1955