p-nitrobenzyloxymethyl: A new fluoride-removable protecting group for ribonucleoside 2′-hydroxyls
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference13 articles.
1. The automated chemical synthesis of long oligoribuncleotides using 2'-O-silylated ribonucleoside 3'-O-phosphoramidites on a controlled-pore glass support: synthesis of a 43-nucleotide sequence similar to the 3'-half molecule of an Escherichia coli formylmethionine tRNA
2. Chemical synthesis of biologically active oligoribonucleotides using β-cyanoethyl protected ribonucleoside phosphoramidites
3. New nucleoside phosphoramidites and coupling protocols for solid-phase RNA synthesis
4. Rapid synthesis of oligoribonucleotides using 2′-O-(o-nitrobenzyloxymethyl)-protected monomers
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3. Development of Bioreduction Labile Protecting Groups for the 2′-Hydroxyl Group of RNA;Organic Letters;2020-07-14
4. Chemical methods for the modification of RNA;Methods;2019-05
5. RNA Synthesis Using the CEM Group;Synthesis of Therapeutic Oligonucleotides;2018
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