New solid-phase for automated synthesis of oligonucleotides containing an amino-alkyl linker at their 3′-end
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference28 articles.
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2. Nonenzymatic sequence-specific cleavage of single-stranded DNA to nucleotide resolution. DNA methyl thioether probes
3. Nonenzymatic sequence-specific cleavage of single-stranded DNA.
4. Complementary addressed reagents carrying EDTA-Fe(II) groups for directed cleavage of single-stranded nucleic acids
5. Phosphorylating agent for the synthesis of oligonucleotide with aliphatic amino group at 5′ end
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1. Development of a 3′-amino linker with high conjugation activity and its application to conveniently cross-link blunt ends of a duplex;Bioorganic & Medicinal Chemistry;2016-05
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. MICROWAVES SYNTHESIS OF SOLID SUPPORTS FOR THE SYNTHESIS OF 3′-AMINOALKYL OLIGODEOXYNUCLEOTIDES;Nucleosides, Nucleotides & Nucleic Acids;2005-04-01
5. Optimized Synthesis of Functionalized Fluorescent Oligodeoxynucleotides for Protein Labeling;Bioconjugate Chemistry;2005-02-24
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