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Oxazole palladium-catalyzed cross-coupling reactions

In contrast, if the mixture of 892 893 was transmetalated at —78°C with ZnCli and the resulting organozinc species quenched with D4-acetic acid, > 85% of the deuterium incorporation was found at C(2). The authors concluded that this organozinc species was best represented as the oxazole 895, which was subsequently used in palladium-catalyzed cross-coupling reactions (see Section 1.4.8). [Pg.194]

TABLE 1.71. 4-( 0-ALKENYL-2-PHENYLOXAZOLES FROM PALLADIUM-CATALYZED CROSS-COUPLING REACTIONS OF 2-PHENYL-4-OXAZOLE TRIFLATE"... [Pg.216]


See other pages where Oxazole palladium-catalyzed cross-coupling reactions is mentioned: [Pg.394]    [Pg.218]    [Pg.326]    [Pg.250]    [Pg.173]    [Pg.287]    [Pg.385]    [Pg.147]    [Pg.116]    [Pg.340]    [Pg.660]   


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Cross palladium

Cross palladium-catalyzed

Cross reactions, palladium-catalyzed

Oxazole reactions

Oxazoles reactions

Palladium coupling

Palladium coupling reaction

Palladium cross-coupling reaction

Palladium-catalyzed coupling

Palladium-catalyzed coupling reaction

Palladium-catalyzed cross-coupling

Palladium-catalyzed cross-coupling reactions

Palladium-catalyzed reactions

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