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    Palladium-Catalyzed Conjugate Addition Type Reaction of Aryl Iodides with alpha,beta-Unsaturated Ketones

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    Aryl iodides have been found to react with alpha,beta-unsaturated ketones in the presence of catalytic amounts of palladium, an excess of formic acid, and triethylamine, giving rise to conjugate addition type products. The electron-withdrawing power of the group attached to the olefinic double bond, the beta substituent to the carbonyl group, and the basic reaction medium appear to affect greatly the conjugate addition/vinylic substitution ratio

    The conversion of vinyl triflates into γ'-hydroxy-α,β-enones

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    Vinyl triflates have been converted into γ'-hydroxy-α,β-enones through their palladium-catalysed coupling with 1-butyn-4-ols followed by the reaction of the obtained 1-hydroxy-3-yn-5-enes in an acidic CH2Cl2/3 N HCl two-phase system in the presence of the n-BuN4Cl/PdCl2 combination. Both the coupling step and the conversion of the carbon-carbon triple bond into the ketonic group have been performed at room temperature. The conversion of vinyl triflates into γ'-hydroxy-α,β-enones can be carried out through a one-flask process, without the isolation of 1-hydroxy-3-yn-5-enes

    A VERSATILE APPROACH TO 2,3-DISUBSTITUTED INDOLES THROUGH THE PALLADIUM-CATALYZED CYCLIZATION OF ORTHO-ALKYNYLTRIFLUOROACETANILIDES WITH VINYL TRIFLATES AND ARYL HALIDES

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    The Palladium-catalyzed cyclization of o-alkynyltrifluoroacetanilides with vinyl triflates and aryl halides produces 2,3-disubstituted indoles in good to high yiel

    PALLADIUM-CATALYZED COUPLING OF ARYL AND VINYL TRIFLATES OR HALIDES WITH 2-ETHYNYLANILINE - AN EFFICIENT ROUTE TO FUNCTIONALIZED 2-SUBSTITUTED INDOLES

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    The Pd-catalysed coupling of the easily available 2-ethynylaniline with aryl and vinyl triflates or halides followed by a Pd(II) catalysed cyclization provides 2-substituted indoles in good yield

    A Novel One-Pot Palladium-Catalysed Synthesis of 2-Aryl- and 2-Vinyl-4H-3,1-benzoxazin-4-ones

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    The palladium-catalysed reaction of o-iodoaniline with unsaturated halides or triflates in the presence of K2CO3 and catalytic amounts of Pd(PPh3)4 under an atmosphere of carbon monoxide affords 2-aryl- and 2-vinyl-4H-3,1-benzoxazin-4-ones in good to high yield
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