Study of Lewis acid accelerated palladium catalyzed CH activation
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文摘
Amide and urea directed ortho-acylation and ortho-olefination on aromatic cores is accelerated by Lewis acidic additives. Lewis acidic additives afford more electrophilic transition metal center, favoring CH activation. The efficiency of several palladium(II) catalysts is raised. KIE experiments and calculations suggests a rate-determining CH activation step.

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