Combinatorial synthesis of 2,9-substituted purines
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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1. Inhibition of Cyclin-Dependent Kinases by Purine Analogues
2. Multiple modes of ligand recognition: Crystal structures of cyclin-dependent protein kinase 2 in complex with ATP and two inhibitors, olomoucine and isopentenyladenine
3. A Structure-Based Library Approach to Kinase Inhibitors
4. Preparation and application of the 5-(4-(9-fluorenylmethyloxycarbonyl)aminomethyl-3,5-dimethoxyphenoxy)-valeric acid (PAL) handle for the solid-phase synthesis of C-terminal peptide amides under mild conditions
5. Regioselective Preparation of 4-Formyl-3,5-dimethoxyphenol, an Intermediate in the Synthesis of the PAL Solid-Phase Peptide Synthesis Handle
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1. Synthesis and screening of 6‐alkoxy purine analogs as cell type‐selective apoptotic inducers in Jurkat cells;Archiv der Pharmazie;2021-06-15
2. 2-Arylamino-6-ethynylpurines are cysteine-targeting irreversible inhibitors of Nek2 kinase;RSC Medicinal Chemistry;2020
3. Solvent-free Synthesis of 2,6-Dihydroxy-9H-purin and Pteridine Derivatives;Journal of Heterocyclic Chemistry;2017-06-20
4. Solid-Phase Synthetic Strategies for the Preparation of Purine Derivatives;ACS Combinatorial Science;2016-06-10
5. Chemistry of Fluorinated Purines;Fluorine in Heterocyclic Chemistry Volume 2;2014
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