7-Functionalized 7-Deazapurine Ribonucleosides Related to 2-Aminoadenosine, Guanosine, and Xanthosine: Glycosylation of Pyrrolo[2,3-d]pyrimidines with 1-O-Acetyl-2,3,5-tri-O-benzoyl-d-ribofuranose
Author:
Affiliation:
1. Laboratorium für Organische und Bioorganische Chemie, Institut für Chemie, Universität Osnabrück, Barbarastr. 7, D-49069 Osnabrück, Germany, and Center for Nanotechnology (CeNTech), Gievenbecker Weg 11, 48149 Münster, Germany
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo0516640
Reference74 articles.
1. Suhadolnik, R. J.PyrrolopyrimidineNucleosides in NucleosideAntibiotics; Wiley-Interscience: New York, 1970; pp 298−353 (and references therein).
2. Structure of the modified nucleoside Q isolated from Escherichia coli transfer ribonucleic acid. 7-(4,5-cis-Dihydroxy-1-cyclopenten-3-ylaminomethyl)-7-deazaguanosine
3. Revankar, G. R.; Robins, R. K. InPyrrolo[2,3-d]pyrimidine(7-Deazapurine) Nucleosides in Chemistry of Nucleosides and Nucleotides; Townsend, L. B., Ed.; Plenum Press: New York, 1991; pp 200−247 (and references therein).
4. Base-Pairing, Tautomerism, and Mismatch Discrimination of 7-Halogenated 7-Deaza-2‘-deoxyisoguanosine: Oligonucleotide Duplexes with Parallel and Antiparallel Chain Orientation
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