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Synthesis of Pyrazolo[1,5-A]Pyridines: [3+2] Cycloaddition of N-Aminopyridines and Enaminones

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inferredcites →https://doi.org/10.1016/s0960-894x(02)00390-6openalex-extracted
Fused Azaindole Derivatives: Molecular Design, Synthesis and In Vitro Pharmacology Leading to the Preferential Dopamine D3 Receptor Agonist FAUC 725
inferredcites →https://doi.org/10.1021/acs.joc.2c02242openalex-extracted
Synthesis of Pyrazolo[1,5-a]pyridinyl, Pyrazolo[1,5-a]quinolinyl, and Pyrazolo[5,1-a]isoquinolinyl Sulfonyl Fluorides via a [3 + 2] Annulation
inferredcites →https://doi.org/10.1021/acs.orglett.2c00035openalex-extracted
Regioselective Synthesis of Pyrazolo[1,5-a]pyridine via TEMPO-Mediated [3 + 2] Annulation–Aromatization ofN-Aminopyridines and α,β-Unsaturated Compounds
inferredcites →https://doi.org/10.1021/ol902710fopenalex-extracted
Synthesis of 2-Substituted Pyrazolo[1,5-a]pyridines through Cascade Direct Alkenylation/Cyclization Reactions
inferredcites →https://doi.org/10.1039/c9ob02668aopenalex-extracted
Copper-mediated oxidative [3 + 2]-annulation of nitroalkenes and pyridinium imines: efficient synthesis of 3-fluoro- and 3-nitro-pyrazolo[1,5- a ]pyridines
inferredcites →https://doi.org/10.1039/d2ob00499bopenalex-extracted
Base-mediated [3 + 2]-cycloannulation strategy for the synthesis of pyrazolo[1,5- a ]pyridine derivatives using ( E )-β-iodovinyl sulfones
inferredcites →https://doi.org/10.1039/d3qo00190copenalex-extracted
N -Amino pyridinium salts in organic synthesis
inferredcites →https://doi.org/10.1080/00397911.2020.1805468openalex-extracted
Pyrazolo[1,5- a ]pyridine: Recent synthetic view on crucial heterocycles
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