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Copper-Catalyzed Bromination of C(spp>3p>)−H Bonds Distal to Functional Groups
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文摘
Selective bromination of γ-methylene C(spp>3p>)−H bonds of aliphatic amides and δ-methylene C(spp>3p>)−H bonds of nosyl-protected alkyl amines are developed using NBS as the brominating reagent and catalytic amount of Cup>IIp>/phenanthroline complexes as the catalyst. Aryl and benzylic C−H bonds at other locations remain intact during this directed radical abstraction reaction.

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