An acid-labile linker for solid-phase oligoribonucleotide synthesis using Fmoc group for 5′-hydroxyl protection
- 26 March 1993
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 34 (13) , 2195-2198
- https://doi.org/10.1016/s0040-4039(00)60380-5
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- The 9-fluorenylmethyloxycarbonyl group as a 5?-OH protection in oligonucleotide synthesisBiopolymers, 1989
- Solid-phase synthesis of oligoribonucleotides using 9-fluorenylmethorycarbunyl (Fmoc) for 5′-hydroryl protectionNucleic Acids Research, 1989
- A new base-stable linker for solid-phase oligonucleotide synthesisJournal of the Chemical Society, Chemical Communications, 1989
- The Problem of 2′-Protection in Rapid Oligoribonucleotide SynthesisNucleosides and Nucleotides, 1987
- The 9-Fluorenylmethyloxycarbonyl (Fmoc) Group as a 5′-O Base Labile Protecting Group in Solid Supported Oligonucleotide SynthesisNucleosides and Nucleotides, 1987
- Solid Phase Synthesis of DNA Under a Non-Depurinating Condition with a Base Labile 5′-Protecting Group (Fmoc) Using Phosphiteamidite ApproachNucleosides and Nucleotides, 1987
- Incompatibility of acid-labile 2′ and 5′ protecting groups for solid-phase synthesis of oligoribonucleotidesTetrahedron Letters, 1986
- Some Aspects of the Chemical Synthesis of OligoribonucleotidesNucleosides and Nucleotides, 1985
- The flouren-9-ylmethoxycarbonyl group for the protection of hydroxy-groups; its application in the synthesis of an octathymidylic acid fragmentJournal of the Chemical Society, Chemical Communications, 1982
- Symmetrical alternative to the tetrahydropyranyl protecting groupJournal of the American Chemical Society, 1967