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Direct carbonylative coupling, palladium chloride

For the ketone synthesis via the present protocol, acid chlorides are useful precursors, in deed. Nevertheless, carbonylative cross coupling with organic halides is strategically the most simple and direct way to this purpose. The palladium-catalyzed carbonylative cross-coupling reaction with various organic halides has been extensively investigated, because of its merits from synthetic as well as phenomenal point of view. Acid chlorides are not always readily available, and their preparation is not always compatible with many sensitive functionalities. Therefore the development of this type of reaction widens the scope of the ketone synthesis in the present protocol because of the ready availability and storability of organic halides and pseudohalides. [Pg.119]


See other pages where Direct carbonylative coupling, palladium chloride is mentioned: [Pg.147]    [Pg.165]    [Pg.212]    [Pg.251]    [Pg.363]    [Pg.212]    [Pg.56]    [Pg.56]    [Pg.75]    [Pg.109]    [Pg.102]    [Pg.53]   


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Carbonyl chlorid

Carbonyl chloride

Carbonylation direct

Carbonylations palladium chloride

Carbonylative coupling

Chlorides carbonylation

Coupling chloride

Couplings direct

Palladium carbonyl chloride

Palladium carbonylation

Palladium carbonylations

Palladium carbonyls

Palladium chloride

Palladium coupling

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