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Benzyl-alkenyl cross-coupling, palladium-catalyzed

The formation of 2-alkenyl-substituted furans was observed in the palladium-catalyzed cross-coupling reactions between benzyl, aryl, or allyl bromides and conjugated ene-yne-ketones. This reaction involved oxidative addition, alkyne activation-cyclization, palladium carbene migratory insertion, P-hydride elimination, and catalyst regeneration (13JA13502). [Pg.202]


See other pages where Benzyl-alkenyl cross-coupling, palladium-catalyzed is mentioned: [Pg.730]    [Pg.315]    [Pg.37]    [Pg.86]    [Pg.317]    [Pg.1754]    [Pg.404]    [Pg.335]    [Pg.71]    [Pg.358]    [Pg.21]   


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Benzyl-alkenyl cross-coupling, palladium-catalyzed benzylation

Benzyl-alkenyl cross-coupling, palladium-catalyzed benzylation

Benzylic palladium catalyzed

Cross palladium

Cross palladium-catalyzed

Palladium alkenylation

Palladium benzylation

Palladium coupling

Palladium-catalyzed benzylation

Palladium-catalyzed coupling

Palladium-catalyzed cross-coupling

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