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RESEARCH PRODUCT

Oligo(1,4-phenylenepyrazole-3,5-diyl)s

A. HormazaHerbert Meier

subject

Methylhydrazinechemistry.chemical_compoundChalconechemistryNucleophileYield (chemistry)Organic ChemistryPolymer chemistryRegioselectivityPhysical and Theoretical ChemistryBenzeneBifunctional

description

The bifunctional nucleophile methylhydrazine reacts in an alkaline medium in a regioselective mode with chalcones to yield 2-pyrazolines, which can be oxidized by DDQ to the corresponding 1H-pyrazoles. From oligo(chalcone)s this reaction yields cross-conjugated compounds with an alternating sequence of 1,4-disubstituted benzene rings and 3,5-disubstituted 1H-pyrazole rings. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003)

https://doi.org/10.1002/ejoc.200300221