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• W2224916178 abstract "This paper reports a novel approach for the direct and facile synthesis of 1,2-oxyamino moieties via an intermolecular copper-catalyzed oxyamination of olefins. This strategy utilizes O -benzoylhydroxylamines as an electrophilic amine source and carboxylic acids as a nucleophilic oxygen source to achieve a modular difunctionalization of olefins. The reaction proceeded in a regioselective manner with moderate to good yields, exhibiting a broad scope of carboxylic acid, amine, and olefin substrates." @default.
• W2224916178 created "2016-06-24" @default.
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• W2224916178 date "2016-01-07" @default.
• W2224916178 modified "2023-10-07" @default.
• W2224916178 title "Copper-catalyzed intermolecular oxyamination of olefins using carboxylic acids and <i>O</i>-benzoylhydroxylamines" @default.
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• W2224916178 doi "https://doi.org/10.3762/bjoc.12.4" @default.
• W2224916178 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4734347" @default.
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