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    Copper-catalyzed synthesis of heterocycle derivatives: use of β-enaminones

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    The use of β-enaminones in synthesis is a subject of great current interest, mostly because of their electronic properties. An appropriate design of the starting β-enaminone could allow for obtaining several classes of heterocyclic derivs. through base- or transition metal-catalyzed reactions. E.g., preparation. of a β-enaminone by reaction of 2-BrC6H4COC≡CPh, followed by addittion of CuI, K2CO3, and DMEDA in DMSO, gave 88% 4-quinolone derivative (I)

    Parallel Palladium-Catalyzed Synthesis of Carboxylic Acids from Aryl Iodides, Bromides, and Vinyl Triflates Using Acetic Anhydride and Formate Anion as an External Condensed Source of Carbon Monoxide

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    Aryl iodides, bromides and vinyl-triflates are usually converted in high to excellent yields into the corresponding carboxylic acids through a parallel palladium-catalyzed hydroxycarbonylation using lithium formate and acetic anhydride as external condensed source of carbon monoxide
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