An efficient access to 3,6-disubstituted 1H-pyrazolo[3,4-b]pyridines via a one-pot double SNAr reaction and pyrazole formation
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference29 articles.
1. Antileishmanial Pyrazolopyridine Derivatives: Synthesis and Structure−Activity Relationship Analysis
2. Design, Synthesis, and Biological Evaluation of AT1 Angiotensin II Receptor Antagonists Based on the Pyrazolo[3,4-b]pyridine and Related Heteroaromatic Bicyclic Systems
3. Synthesis and evaluation of pyrazolo[3,4-b]pyridine CDK1 inhibitors as anti-tumor agents
4. SYNTHESIS AND BIOLOGICAL EVALUATION OF 1H-PYRAZOLO [3,4-b] PYRIDINE-5 CARBOXYLIC ACIDS AGAINST VACCINIA VIRUS
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1. Tandem Oxidative Reaction of 1,3-Diarylpropenes and 5-Aminopyrazoles;Synlett;2023-07-31
2. Facile Preparation of 3-Substituted-2,6-difluoropyridines and Application to the Synthesis of 2,3,6-Trisubstituted Pyridines for PKCθ Inhibitors;Journal of Synthetic Organic Chemistry, Japan;2020-02-01
3. An efficient synthesis of fully substituted pyrazolo[3,4-b]pyridin-5-amines from α-azidochalcones;Tetrahedron;2018-05
4. Convenient Synthesis of Spirooxindole-Fused Pyrazolopyridine Derivatives;ChemistrySelect;2018-02-12
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