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Nickel-Catalyzed Asymmetric Arylation of H-Phosphinates

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GEORG THIEME VERLAG KG
DOI: 10.1055/s-0042-1751456

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phosphinates; P-stereogenic centers; nickel catalysis; cross-coupling; asymmetric catalysis

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An asymmetric arylation of H-phosphinates with aromatic iodo or bromo compounds, catalyzed by cheap and easily available nickel(II) salts, allows the synthesis of P-stereogenic phosphinates. This method offers mild reaction conditions and good functional-group compatibility including aniline and phenol derivatives.
An asymmetric arylation of H-phosphinates with aromatic iodo or bromo compounds, catalyzed by cheap and easily available nick-el(II) salts, provides access to P-stereogenic phosphinates. This method features mild reaction conditions and a good functional-group compat-ibility that includes aniline and phenol derivatives.

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