Solid phase synthesis of 5',3'-bifunctional oligodeoxyribonucleotides bearing a masked thiol group at the 3'-end
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference9 articles.
1. Antisense oligonucleotides: a new therapeutic principle
2. Specific regulation of gene expression by antisense, sense and antigene nucleic acids
3. Efficient methods for attachment of thiol specific probes to the 3′-ends of synthetic oligodeoxyribonucleotides
4. A universal solid support for the synthesis of 3′-thiol group containing oligonucleotides
5. Thin layer chromatography: Silica gel plates (Merck DC Alufolien Kieselgel, 60 F 254), solvent: CH2Cl2/MeOH 90:10 V/V.
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1. Disulfide bridge as a linker in nucleic acids’ bioconjugation. Part I: An overview of synthetic strategies;Bioorganic Chemistry;2019-11
2. Preparation of a disulfide-linked precipitative soluble support for solution-phase synthesis of trimeric oligodeoxyribonucleotide 3´-(2-chlorophenylphosphate) building blocks;Beilstein Journal of Organic Chemistry;2015-09-07
3. Solid‐Phase Supports for Oligonucleotide Synthesis;Current Protocols in Nucleic Acid Chemistry;2013-06
4. ChemInform Abstract: Solid Phase Synthesis of 5′,3′-Bifunctional Oligodeoxyribonucleotides Bearing a Masked Thiol Group at the 3′-End.;ChemInform;2010-08-22
5. Enzyme-Free Interrogation of RNA Sites via Primers and Oligonucleotides 3‘-Linked to Gold Surfaces;Organic Letters;2007-05-01
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