6533b85ffe1ef96bd12c19ca
RESEARCH PRODUCT
Oligo(1,4-phenylenepyrazole-3,5-diyl)s
A. HormazaHerbert Meiersubject
Methylhydrazinechemistry.chemical_compoundChalconechemistryNucleophileYield (chemistry)Organic ChemistryPolymer chemistryRegioselectivityPhysical and Theoretical ChemistryBenzeneBifunctionaldescription
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)
year | journal | country | edition | language |
---|---|---|---|---|
2003-09-01 | European Journal of Organic Chemistry |