Solid-phase synthesis of modified oligodeoxyribonucleotides with an acridine derivative or a thiophosphate group at their 3′end
- 1 January 1989
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 30 (19) , 2521-2524
- https://doi.org/10.1016/s0040-4039(01)80440-8
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Efficient methods for attachment of thiol specific probes to the 3′-ends of synthetic oligodeoxyribonucleotidesNucleic Acids Research, 1987
- Synthese et reactivite d'oligothymidylates substitues par un agent intercalant et un groupe thiophosphateTetrahedron Letters, 1987
- Solid phase 5′-phosphorylation of oligonucleotidesTetrahedron Letters, 1987
- New Approach to the Synthesis of Deoxyribonucleoside Phosphoramidite DerivativesChemistry Letters, 1986
- Oligothymidylates Substitubs en Position 3’ Par un Derive De L'AcridineNucleosides, Nucleotides and Nucleic Acids, 1986
- Nucleic acid-binding molecules with high affinity and base sequence specificity: intercalating agents covalently linked to oligodeoxynucleotides.Proceedings of the National Academy of Sciences, 1984
- Oligodeoxynucleotides covalently linked to intercalating dyes as base sequence-specific ligands. Influence of dye attachment site.The EMBO Journal, 1984
- Deoxynucleoside phosphoramidites—A new class of key intermediates for deoxypolynucleotide synthesisTetrahedron Letters, 1981