Reactivity of the –C(Cl)C–CN– moiety towards AlCl3-induced C–C bond forming reactions: a new synthesis of 7-(hetero)aryl-substituted pyrazolo[1,5-a]pyrimidines
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference26 articles.
1. Synthesis and antischistosomal activity of certain pyrazolo[1,5-a]pyrimidines
2. Novel heterocyclic nitrofurfural hydrazones. In vivo antitrypanosomal activity
3. Optimization of a pyrazolo[1,5-a]pyrimidine class of KDR kinase inhibitors: improvements in physical properties enhance cellular activity and pharmacokinetics
4. Synthesis and biological evaluations of condensed pyridine and condensed pyrimidine-based HMG-CoA reductase inhibitors
5. Synthesis and SAR of a New Series of COX-2-Selective Inhibitors: Pyrazolo[1,5-a]pyrimidines
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1. D-π-A-Type Pyrazolo[1,5-a]pyrimidine-Based Hole-Transporting Materials for Perovskite Solar Cells: Effect of the Functionalization Position;Materials;2022-11-11
2. Synthesis of novel 3-(quinazol-2-yl)-quinolines via SNAr and aluminum chloride-induced (hetero) arylation reactions and biological evaluation as proteasome inhibitors;Tetrahedron Letters;2020-04
3. A Parallel Approach to 7-(Hetero)arylpyrazolo[1,5-a]pyrimidin-5-ones;ACS Combinatorial Science;2018-04-04
4. Ultrasound-Assisted 3-Component Reaction in Acetic Acid Alone: Catalyst / Promoter / Ligand Free Synthesis of Bioactive Pyrazolo[1,5-a]pyrimidines;Letters in Drug Design & Discovery;2017-09-08
5. Use of AlCl3 in Friedel Crafts arylation type reactions and beyond: an overview on the development of unique methodologies leading to N-heteroarenes;Organic & Biomolecular Chemistry;2017
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