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- W2320365564 endingPage "5285" @default.
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- W2320365564 abstract "Palladium-catalyzed intermolecular C–N bond-forming reactions between aryl halides and amides are described using 2-dialkylphosphino-2′-alkoxyl-1,1′-binaphthyl, which is both bulky and electron-rich, as the ligand. A variety of amides, including aliphatic and aromatic primary amides, lactams, and carbamates, were viable substrates for the amidation, which exhibited good functional group compatibility. By tuning the substituents at the 2,2′-position of 1,1′-binaphthyl of the ligand, the palladium-catalyzed amidation of bulky aryl halides was realized and this coupling reaction was used to synthesize 2-amino-2′-methoxy-1,1′-binaphthyl in high yield." @default.
- W2320365564 created "2016-06-24" @default.
- W2320365564 creator A5026125673 @default.
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- W2320365564 creator A5073034733 @default.
- W2320365564 creator A5087696539 @default.
- W2320365564 date "2012-05-31" @default.
- W2320365564 modified "2023-10-12" @default.
- W2320365564 title "Palladium-Catalyzed Amidation of Aryl Halides Using 2-Dialkylphosphino-2′-alkoxyl-1,1′-binaphthyl as Ligands" @default.
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- W2320365564 doi "https://doi.org/10.1021/jo3005827" @default.
- W2320365564 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/22624625" @default.
- W2320365564 hasPublicationYear "2012" @default.
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