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- W2014717734 abstract "An efficient procedure for the trapping of an imidazole-4,5-quinodimethane intermediate 3 with quinones in boiling toluene and in the presence of 18-crown-6 is described. In all cases the fully aromatized imidazole-naphthoquinone derivatives were isolated as the main reaction products in satisfactory yields. However, in the case of benzo- and naphthoquinone, aromatized products were also isolated, in which the bromine in the 2-imidazole position was replaced by hydrogen, whereas in the case of the asymmetrical 2-phenylbenzoquinone and 5,8-quinoline dione inseparable regioisomeric mixtures were formed." @default.
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- W2014717734 date "2007-10-01" @default.
- W2014717734 modified "2023-10-18" @default.
- W2014717734 title "A Versatile One-Pot Synthesis of Fused Polycyclic Imidazole-naphthoquinone Derivatives through Imidazole-4,5-quinodimethane Generation Followed by Diels-Alder Cycloaddition" @default.
- W2014717734 doi "https://doi.org/10.1055/s-2007-986656" @default.
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