Ribosidierung von Pyrrolo[2,3‐ d ]pyrimidinen in Gegenwart starker Basen
Author:
Affiliation:
1. Universität Paderborn – Gesamthochschule, Fachbereich Naturwissenschaften II (Organische Chemie), Warburger Str. 100, D‐4790 Paderborn
Publisher
Wiley
Subject
Inorganic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.19801130826
Reference18 articles.
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4. Bevorzugte O ‐Glycosidbildung bei der Ribosidierung von 5‐Methyl‐2‐methylthio‐7 H ‐pyrrolo[2,3‐ d ]pyrimidin‐4(3 H )‐on
5. 4‐Amino‐7‐(β‐ D ‐arabinofuranosyl)pyrrolo[2,3‐ d ]pyrimidin — die Synthese von Ara‐Tubercidin durch Phasentransferkatalyse
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4. Nucleosides Part LXVI I[ ]: Synthesis of 4-Amino-7(8H)Pteridinone-N8-Nucleosides—Structural Analogs of Adenosine;Nucleosides, Nucleotides & Nucleic Acids;2009-07-29
5. Studies on the Glycosylation of Pyrrolo[2,3-d] Pyrimidines with 1-O-Acetyl-2,3,5-Tri-O-Benzoyl-β-D-Ribofuranose: The Formation of Regioisomers During Toyocamycin and 7-Deazainosine Syntheses;Nucleosides, Nucleotides & Nucleic Acids;2009-07-29
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