The use of labile base protecting groups in oligoribonucleotide synthesis
- 31 December 1989
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 30 (1), 71-74
- https://doi.org/10.1016/s0040-4039(01)80326-9
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
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- The final deprotection step in oligonucleotide synthesis is reduced to a mild and rapid ammonia treatment by using labile base-protecting groupsNucleic Acids Research, 1987
- An Improved Procedure for the Protection of 2′-DeoxyguanosineSynthesis, 1986
- Polymer support oligonucleotide synthesis XVIII1.2): use ofβ-cyanoethyi-N,N-dialkylamino-/N-morpholino phosphoramidite of deoxynucleosides for the synthesis of DNA fragments simplifying deprotection and isolation of the final productNucleic Acids Research, 1984
- In situactivation of bis-dialkylaminophosphines—a new method for synthesizing deoxyoligonucleotides on polymer supportsNucleic Acids Research, 1984
- Transient protection: efficient one-flask syntheses of protected deoxynucleosidesJournal of the American Chemical Society, 1982
- The synthesis of oligoribonucleotides. III. The use of silyl protecting groups in nucleoside and nucleotide chemistry. VIIICanadian Journal of Chemistry, 1979
- Studies on Polynucleotides. XXIV.1 The Stepwise Synthesis of Specific Deoxyribopolynucleotides (4).2 Protected Derivatives of Deoxyribonucleosides and New Syntheses of Deoxyribonucleoside-3″ Phosphates3Journal of the American Chemical Society, 1963