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Direct asymmetric aminoxylation reaction catalyzed by axially chiral amino acids

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CHEMISTRY LETTERS
卷 37, 期 3, 页码 250-251

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CHEMICAL SOC JAPAN
DOI: 10.1246/cl.2008.250

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Binaphthyl-based amino acids were prepared and applied for the direct asymmetric aminoxylation of aldehydes with nitrosobenzene. The reaction catalyzed by (S)-1e proceeded smoothly to give the aminoxylated product in good yield and enantioselectivity. This method represents a rare example of the direct asymmetric aminoxylation by a non-proline-type catalyst.

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