Synthesis of the aminocyclopentenediol fragment of queuosine by way of the stereoselective addition of an organometallic reagent to a N-t-butanesulfinyl glycosylamine
Author:
Affiliation:
1. Institute of Organic and Analytical Chemistry, UMR 7311, University of Orleans and CNRS, Rue de Chartres, 45067 Orleans, France
Abstract
Funder
European Regional Development Fund
Agence Nationale de la Recherche
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2024/OB/D3OB01713C
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1. Amber Suppression: a Nucleotide Change in the Anticodon of a Tyrosine Transfer RNA
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. The structure of Q* nucleoside isolated from rabbit liver transfer ribonucleic acid
4. Stereochemistry of the cyclopentene side chain in the nucleoside Q obtained from tRNA
5. Synthesis of Galactosyl‐Queuosine and Distribution of Hypermodified Q‐Nucleosides in Mouse Tissues
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