Design and Synthesis of Triazolyl‐Donor/Acceptor Unnatural Nucleosides and Oligonucleotide Probes Containing Triazolyl‐Phenanthrene Nucleoside
Author:
Affiliation:
1. Bio‐organic Chemistry Laboratory, Department of Chemistry, Indian Institute of Technology Guwahati Assam‐781039 India
Publisher
Wiley
Subject
General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/0471142700.nc0132s58
Reference35 articles.
1. Installation/Modulation of the Emission Response via Click Reaction
2. Triazolyl Donor/Acceptor Chromophore Decorated Unnatural Nucleosides and Oligonucleotides with Duplex Stability Comparable to That of a Natural Adenine/Thymine Pair
3. Unnatural triazolyl nucleoside stabilizes an abasic site containing DNA duplex equally as the stabilization of a natural A–T pair
4. Dual door entry to exciplex emission in a chimeric DNA duplex containing non-nucleoside–nucleoside pair
5. Bipyridyl- and Biphenyl-DNA: A Recognition Motif Based on Interstrand Aromatic Stacking
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1. Sonogashira Cross-Coupling: Alkyne-Modified Nucleosides and Their Applications ☆;Palladium-Catalyzed Modification of Nucleosides, Nucleotides and Oligonucleotides;2018
2. Regioselective and stereoselective route to N2-β-tetrazolyl unnatural nucleosides via SN2 reaction at the anomeric center of Hoffer’s chlorosugar;Bioorganic & Medicinal Chemistry Letters;2016-04
3. Donor/acceptor chromophores-decorated triazolyl unnatural nucleosides: synthesis, photophysical properties and study of interaction with BSA;Organic & Biomolecular Chemistry;2016
4. Triazolo-β-aza-ε-amino acid and its aromatic analogue as novel scaffolds for β-turn peptidomimetics;Chemical Communications;2015
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