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Biaryl-like CATPHOS diphosphines via double Diels-Alder cycloaddition between 1,4-bis(diphenylphosphinoyl)buta-1,3-diyne and anthracenes:: Efficient ligands for the palladium-catalyzed amination of aromatic bromides and α-arylation of ketones

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ORGANOMETALLICS
卷 27, 期 8, 页码 1679-1682

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AMER CHEMICAL SOC
DOI: 10.1021/om800118t

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A mixture of palladium(0) and CATPHOS, the 1,3-butadiene-bridged diphosphine generated via double Diels-Alder cycloaddition between bis(diphenylphosphinoyl)butci-1,3-diyne and anthracene, catalyzes the amination of a range of aromatic bromides as well as the alpha-arvlation of ketones, giving conversions that either rival or exceed those obtained with BINAP.

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