Mannich‐Reaktion am 2‐Amino‐3,7‐dihydropyrrolo[2,3‐ d ]‐pyrimidin‐4‐on, dem Chromophor des Ribonucleosids „Q”︁
Author:
Affiliation:
1. Universität Paderborn — Gesamthochschule, Fachbereich 13 (Organische Chemie), Pohlweg 55, D‐4790 Paderborn
2. Max‐Planck‐Institut für experimentelle Medizin, Abteilung Chemie, Hermann‐Rein‐Straße 3, D‐3400 Göttingen
Publisher
Wiley
Subject
Inorganic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.19771100428
Reference11 articles.
1. Structure of the modified nucleoside Q isolated from Escherichia coli transfer ribonucleic acid. 7-(4,5-cis-Dihydroxy-1-cyclopenten-3-ylaminomethyl)-7-deazaguanosine
2. Distribution of the modified nucleoside Q and its derivatives in animal and plant transfer RNA's
3. Biosynthesis of the modified nucleoside Q in transfer RNA
4. Pyrrolopyrimidine nucleosides. III. Total synthesis of toyocamycin, sangivamycin, tubercidin, and related derivatives
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