O 6 ‐(Benzotriazol‐1‐yl)inosine Derivatives for C6 Modification of Purine Nucleosides
Author:
Affiliation:
1. The City College and The City University of New York New York
2. PrimeSyn Lab Hillsborough New Jersey
Publisher
Wiley
Subject
General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/0471142700.nc0122s36
Reference34 articles.
1. New, ionic side-products in oligonucleotide synthesis: formation and reactivity of fluorescent N-/purin-6-yl/pyridinium salts1
2. A Chemical Method for Site-Specific Modification of RNA: The Convertible Nucleoside Approach
3. Alkylation of 6-N-acylated adenosine derivatives by the use of phase transfer catalysis
4. O6-(Benzotriazol-1-yl)inosine Derivatives: Easily Synthesized, Reactive Nucleosides
5. Unusual Deoxygenation and Reactivity Studies Related to O6-(Benzotriazol-1-yl)inosine Derivatives
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1. New aromatic 6-substituted 2′-deoxy-9-(β)-d-ribofuranosylpurine derivatives as potential plant growth regulators;Bioorganic & Medicinal Chemistry;2020-01
2. Synthesis and Evaluations of “1,4‐Triazolyl Combretacoumarins” and Desmethoxy Analogs;European Journal of Organic Chemistry;2019-08-07
3. Facile Modifications at the C4 Position of Pyrimidine Nucleosides via In Situ Amide Activation with 1 H ‐Benzotriazol‐1‐yloxy‐tris(dimethyl‐amino)phosphonium Hexafluorophosphate;Current Protocols in Nucleic Acid Chemistry;2019-01-28
4. Facile functionalization at the C4 position of pyrimidine nucleosides via amide group activation with (benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate (BOP) and biological evaluations of the products;Organic & Biomolecular Chemistry;2017
5. Two‐Step, One‐Pot Synthesis of Inosine, Guanosine, and 2′‐Deoxyguanosine O 6 ‐Ethers via Intermediate O 6 ‐(Benzotriazol‐1‐yl) Derivatives;Current Protocols in Nucleic Acid Chemistry;2012-06
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