Oligodeoxynucleotide probes with multiple labels linked to the 4′-position of thymidine monomers: Excellent duplex stability and detection sensitivity
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. The Functionalization of Oligonucleotides Via Phosphoramidite Derivatives
2. Engineering tethered DNA molecules by the convertible nucleoside approach
3. A New Multiple Labelling Method for Synthetic Oligonucleotides and Increased Sensitivity in DNA Detection
4. Oligonucleotide labeling methods 3. Direct labeling of oligonucleotides employing a novel, non-nucleosidic, 2-aminobutyl-1,3-propanediol backbone
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1. 4′-C-[(4-Trifluoromethyl-1H-1,2,3-triazol-1-yl)methyl]thymidine as a Sensitive 19F NMR Sensor for the Detection of Oligonucleotide Secondary Structures;The Journal of Organic Chemistry;2014-04-10
2. ChemInform Abstract: Oligodeoxynucleotide Probes with Multiple Labels Linked to the 4′- Position of Thymidine Monomers: Excellent Duplex Stability and Detection Sensitivity;ChemInform;2010-08-18
3. Synthesis of Conformationally Locked Carba-LNAs through Intramolecular Free-Radical Addition to C═N. Electrostatic and Steric Implication of the Carba-LNA Substituents in the Modified Oligos for Nuclease and Thermodynamic Stabilities;The Journal of Organic Chemistry;2009-08-11
4. Utilization of Intrachain 4′-C-Azidomethylthymidine for Preparation of Oligodeoxyribonucleotide Conjugates by Click Chemistry in Solution and on a Solid Support;Bioconjugate Chemistry;2008-08-01
5. Design, Synthesis, and Properties of 2‘,4‘-BNANC: A Bridged Nucleic Acid Analogue;Journal of the American Chemical Society;2008-03-15
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