N-Phenoxyacetylated guanosine and adenosine phosphoramidites in the solid phase synthesis of oligoribonucleotides: Synthesis of a ribozyme sequence
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference9 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. A small catalytic oligoribonucleotide
3. BIOLOGICAL CATALYSIS BY RNA
4. Splicing of Messenger RNA Precursors
5. The final deprotection step in oligonucleotide synthesis is reduced to a mild and rapid ammonia treatment by using labile base-protecting groups
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1. Regioselective 2′‐Silylation of Purine Ribonucleosides for Phosphoramidite RNA Synthesis;Current Protocols;2023-01
2. An evaluation of selective deprotection conditions for the synthesis of RNA on a light labile solid support;Bioorganic & Medicinal Chemistry Letters;2014-05
3. Preparation of Oligodeoxyribonucleotides Containing the Pyrimidine(6–4)pyrimidone Photoproduct by Using a Dinucleotide Building Block;Current Protocols in Nucleic Acid Chemistry;2013-06
4. Solid-phase synthesis of RNA via a silyl-protecting-group strategy;Recueil des Travaux Chimiques des Pays-Bas;2010-09-02
5. Synthesis of Nucleotidylated Poliovirus VPg Proteins;The Journal of Organic Chemistry;2010-07-22
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