A New 5′-Protecting Group for Use in Solid-Phase Synthesis of Oligoribonucleotides
Author:
Publisher
Informa UK Limited
Subject
Genetics,Biochemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/07328318708056217
Reference13 articles.
1. Oligoribonucleotide synthesis 2′,5′-protected ribonucleoside derivatives
2. Symmetrical alternative to the tetrahydropyranyl protecting group
3. Incompatibility of acid-labile 2′ and 5′ protecting groups for solid-phase synthesis of oligoribonucleotides
4. The 9-phenylxanthen-9-yl protecting group
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1. Synthesis of Branched DNA Using Oxidatively Cleavable Tritylsulfenyl as a Hydroxy Protecting Group;Current Protocols in Nucleic Acid Chemistry;2014-09
2. Synthesis of oligodeoxynucleotides using the oxidatively cleavable 4-methoxytritylthio (MMTrS) group for protection of the 5′-hydroxyl group;New Journal of Chemistry;2010
3. New Protected Protecting Groups for the 5′-Hydroxy Group of Deoxynucleosides by Use of 2-(Hydroxymethyl)- and 2-[(Methylamino)methyl]benzoyl Skeletons and Oxidatively Cleavable Tritylthio and (4-Methoxytrityl)thio Groups;Helvetica Chimica Acta;2004-09
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. Synthesis of pentathymidylate using a 4-monomethoxytritylthio (MMTrS) group as a 5′-hydroxyl protecting group: toward oligonucleotide synthesis without acid treatment;Tetrahedron Letters;2001-12
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