Publication | Closed Access
Solid‐Phase Synthesis of Substituted Pyrazolones from Polymer‐Bound β‐Keto Esters
14
Citations
8
References
2001
Year
EngineeringPolymer-bound Acetoacetate 3Organic ChemistryHeterocycle ChemistryPyrazolones 17A−ddAcidic Cyclizing CleavagePharmacologySynthesis MethodSynthetic ChemistryBiomolecular EngineeringSolid‐phase SynthesisNatural Product Synthesis
Polymer-bound acetoacetate 3 was γ-mono- and γ-dialkylated, as well as α-monoalkylated, to give 6, 9, and 13, respectively. Treatment with hydrazine or substituted hydrazines followed by thermal or acidic cyclizing cleavage yielded the pyrazolones 17a−dd in a purity of >90%.
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