Synthese und Eigenschaften von 5′‐Desoxynucleosid‐5′‐carbonsäuren und ihren Derivaten
Author:
Affiliation:
1. Fachbereich Chemie der Universität Marburg, Hans‐Meerwein‐Str., D‐3550 Marburg
Publisher
Wiley
Subject
Inorganic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.19801130719
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4. Design of substrate-site-directed irreversible inhibitors of adenosine 5'-phosphate aminohydrolase. Effect of substrate substituents on affinity for the substrate site
5. Adenine Nucleosides in Solution: Stabilisation of the anti-Conformation by C-5' Substituents
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1. Inactivation of S-adenosylhomocysteine hydrolase with haloethyl and dihalocyclopropyl esters derived from homoadenosine-6′-carboxylic acid;Bioorganic & Medicinal Chemistry Letters;2004-12
2. Synthesis of a thymidine dimer containing a tetrazole-2,5-diyl internucleosidic linkage and its insertion into oligodeoxynucleotides;Helvetica Chimica Acta;2002-09
3. Synthesis of Homologated Halovinyl Derivatives from Aristeromycin and Their Inhibition of Human Placental S-Adenosyl-L-homocysteine Hydrolase;Nucleosides, Nucleotides and Nucleic Acids;1998-01-01
4. Mechanism of Inactivation of S-Adenosylhomocysteine Hydrolase by (E)-5',6'-Didehydro-6'-deoxy-6'-halohomoadenosines;Biochemistry;1994-03
5. Application of Ultrasonic Waves: An Improved Synthesis of 5′-Deoxy-5′-cyano-2′,3′-isopropylidene Adenosine;Synthetic Communications;1990-12
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