An acid-labile linker for solid-phase oligoribonucleotide synthesis using Fmoc group for 5′-hydroxyl protection
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference15 articles.
1. Some Aspects of the Chemical Synthesis of Oligoribonucleotides
2. The Problem of 2′-Protection in Rapid Oligoribonucleotide Synthesis
3. Symmetrical alternative to the tetrahydropyranyl protecting group
4. Incompatibility of acid-labile 2′ and 5′ protecting groups for solid-phase synthesis of oligoribonucleotides
5. The flouren-9-ylmethoxycarbonyl group for the protection of hydroxy-groups; its application in the synthesis of an octathymidylic acid fragment
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1. ChemInform Abstract: An Acid-Labile Linker for Solid-Phase Oligoribonucleoside Synthesis Using Fmoc Group for 5′-Hydroxyl Protection.;ChemInform;2010-09-01
2. A solid-phase approach to the synthesis of N-1-alkyl analogues of cyclic inosine-diphosphate-ribose (cIDPR);Tetrahedron;2010-03
3. Solid-Phase Synthesis of Nucleoside Analogues;Journal of Combinatorial Chemistry;2003-03-11
4. Reactions at Oxygen Atoms;Glycoscience: Chemistry and Chemical Biology I–III;2001
5. A solid-phase approach to analogues of the antibiotic mureidomycin;Bioorganic & Medicinal Chemistry Letters;2000-12
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