Two‐Step, One‐Pot Synthesis of Inosine, Guanosine, and 2′‐Deoxyguanosine O 6 ‐Ethers via Intermediate O 6 ‐(Benzotriazol‐1‐yl) Derivatives
Author:
Affiliation:
1. The City College and The City University of New York New York City New York
Publisher
Wiley
Subject
General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/0471142700.nc0126s49
Reference45 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. Synthesis of a new class of spin-labeled purine ribonucleosides and development of a novel nucleophilic reaction to form 2,6,8-trifunctionalized purine derivatives
4. O 6 ‐(Benzotriazol‐1‐yl)inosine Derivatives for C6 Modification of Purine Nucleosides
5. O6-(Benzotriazol-1-yl)inosine Derivatives: Easily Synthesized, Reactive Nucleosides
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1. 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
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