4.6 Article

Asymmetric Michael addition of aldehydes to nitroalkenes using a primary amino acid lithium salt

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ORGANIC & BIOMOLECULAR CHEMISTRY
卷 8, 期 13, 页码 3031-3036

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ROYAL SOC CHEMISTRY
DOI: 10.1039/c003940c

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  1. Ministry of Education, Culture, Sports, Science and technology, Japan [B01]

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Enantioselective Michael addition of aldehydes to nitroalkenes was successfully carried out by asymmetric catalysis with L-phenylalanine lithium salt, giving gamma-nitroaldehydes in good yields with high enantioselectivity.

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