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A Novel Reaction of the “Huisgen Zwitterion” with Chalcones and Dienones: An Efficient Strategy for the Synthesis of Pyrazoline and Pyrazolopyridazine Derivatives
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Citations
14
References
2007
Year
Pyrazolopyridazine DerivativesDerivativesBioorganic ChemistryEngineeringHuisgen ZwitterionNatural SciencesNovel ReactionUnexpected TransformationsOrganic ChemistryExcess DiadEfficient StrategyChemistryHeterocycle ChemistryPharmacologyDerivative (Chemistry)Synthetic ChemistryBiomolecular Engineering
Two unexpected transformations: The reaction of the Huisgen zwitterion derived from triphenylphosphane and diisopropyl azodicarboxylate (DIAD) with chalcones affords functionalized pyrazolines. In contrast, the reaction with dienones affords pyrazolopyridazines, presumably by Diels–Alder reaction of the initially formed pyrazoline with excess DIAD (see scheme). Supporting information for this article is available on the WWW under http://www.wiley-vch.de/contents/jc_2002/2007/z604025_s.pdf or from the author. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
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