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- W2917237357 abstract "Abstract The reductive Barbier coupling of aromatic halides and electrophiles has been achieved using a CoBr 2 /1,10‐phenanthroline catalytic system and over stoichiometric amounts of zinc. The reaction displayed a broad scope of substrates, including (hetero)aryl chlorides as pro‐nucleophiles and aldehydes or imines as electrophiles, leading to diarylmethanols and diarylmethylamines in moderate to excellent yields, respectively." @default.
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- W2917237357 date "2019-02-22" @default.
- W2917237357 modified "2023-10-12" @default.
- W2917237357 title "Co <sup>I</sup> ‐Catalyzed Barbier Reactions of Aromatic Halides with Aromatic Aldehydes and Imines" @default.
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- W2917237357 doi "https://doi.org/10.1002/chem.201806239" @default.
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