Multicomponent Synthesis of α-Branched Amides

ORGANIC LETTERS(2009)

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摘要
alpha-Branched amides are prepared by multicomponent reactions in which nitriles undergo hydrozirconation to form metalloimines that react with acyl chlorides. The resulting acylimines react with a variety of pi-nucleophiles in the presence of Lewis acids to form the desired amides.
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