Incompatibility of acid-labile 2′ and 5′ protecting groups for solid-phase synthesis of oligoribonucleotides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference13 articles.
1. Oligoribonucleotide synthesis 2′,5′-protected ribonucleoside derivatives
2. Symmetrical alternative to the tetrahydropyranyl protecting group
3. The protection of 2′-hydroxy functions in oligoribonucleotide synthesis
4. The 9-phenylxanthen-9-yl protecting group
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1. Protection for the Hydroxyl Group, Including 1,2- and 1,3-Diols;Greene's Protective Groups in Organic Synthesis;2014-08-11
2. Protective groups in the chemical synthesis of oligoribonucleotides;Russian Journal of Bioorganic Chemistry;2013-01
3. Novel Base-Labile Protecting Groups for 5′-Hydroxy Function in Solid-Phase Oligonucleotide Synthesis;Nucleosides, Nucleotides and Nucleic Acids;2003-10
4. 6-(Levulinyloxymethyl)-3-methoxy-2-nitrobenzoyl and 2-(Levulinyloxymethyl)-5-methoxy-4-nitrobenzoyl Groups as Novel Base-Labile Groups for 5′-Hydroxy Protection in Solid-Phase Oligonucleotide Synthesis;Nucleosides, Nucleotides & Nucleic Acids;2003-07-01
5. RNA Oligonucleotide Synthesis via 5′-Silyl-2′-Orthoester Chemistry;Methods;2001-03
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