Publication | Closed Access
A Phosphine-Catalyzed Preparation of 4-Arylidene-5-imidazolones
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Citations
22
References
2014
Year
Robust RouteHeterocyclicBiochemistryNatural SciencesPhosphine-catalyzed PreparationOrganic ChemistrySynthetic ChemistryIntramolecular CyclizationChemistryHeterocycle ChemistryPharmacologyAmidine Pronucleophiles
A simple and efficient method for constructing 4-arylidene-5-imidazolones was developed using a phosphine-catalyzed tandem umpolung addition and intramolecular cyclization of amidine pronucleophiles on arylpropiolates. The reaction offers a robust route to heterocycle analogues of the fluorescent protein chromophores.
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