Incompatibility of acid-labile 2′ and 5′ protecting groups for solid-phase synthesis of oligoribonucleotides
- 1 January 1986
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 27 (13) , 1521-1522
- https://doi.org/10.1016/s0040-4039(00)84302-6
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- 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
- A NEW PROTECTING TACTICS FOR THE URACIL RESIDUE IN OLIGORIBONUCLEOTIDE SYNTHESISChemistry Letters, 1983
- Hindered dialkylamino nucleoside phosphite reagents in the synthesis of two DNA 51-mersJournal of the American Chemical Society, 1983
- The 9-phenylxanthen-9-yl protecting groupJournal of the Chemical Society, Chemical Communications, 1978
- The Synthesis of oligoribonucleotides—IVTetrahedron, 1968
- Symmetrical alternative to the tetrahydropyranyl protecting groupJournal of the American Chemical Society, 1967
- Oligoribonucleotide synthesisTetrahedron Letters, 1964
- 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