Lithiation of 1H-pyrazolo[3,4-d]pyrimidine derivative using lithium alkanetellurolate
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference5 articles.
1. Triazolo[4,5-d]pyrimidines. X. Halogen-Metal Exchange Reaction of 7-Halo-3-phenyl-3H-1,2,3-triazolo[4,5-d]pyrimidines with Butyllithium.
2. A new access to acyl- and aroyllithiums via lithium-tellurium exchange
3. Lithium-Tellurium Exchange: A New Entry to Organolithium Compounds
4. Carbamoyllithiums. A Novel Method for Generation by Lithium-Tellurium Exchange Reaction
5. Preparation and reactions of 2-pyridyltellurium derivatives
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1. Human dihydrofolate reductase inhibition effect of 1-Phenylpyrazolo[3,4–d]pyrimidines: Synthesis, antitumor evaluation and molecular modeling study;Bioorganic Chemistry;2022-12
2. Design, synthesis and antitumor evaluation of novel pyrazolo[3,4-d]pyrimidines incorporating different amino acid conjugates as potential DHFR inhibitors;Journal of Enzyme Inhibition and Medicinal Chemistry;2022-11-16
3. Synthesis and Characterization of 2-Fluoro-3-Pyridyl Tellurium Compounds: X-Ray Crystal Structure of Bis(2-Fluoro-3-Pyridyltelluro)Methane;Phosphorus, Sulfur, and Silicon and the Related Elements;2015-08-17
4. Preparation and characterization of symmetrical bis[4-chloro-2-pyrimidyl] dichalcogenide (S, Se, Te) and unsymmetrical 4-chloro-2-(arylchalcogenyl) pyrimidine: X-ray crystal structure of 4-chloro-2-(phenylselanyl) pyrimidine and 2-(p-tolylselanyl)-4-chloropyrimidine;Journal of Organometallic Chemistry;2011-02
5. Non-Deprotonating Methodologies for Organolithium Reagents Starting from Non-Halogenated Materials. Part 1: Carbon – Heteroatom Bond Cleavage;Current Organic Chemistry;2011-02-01
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