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• W1963599686 abstract "Arylacetonitriles are able to participate in organocatalytic Michael additions to α,β-unsaturated aldehydes by incorporating a nitro group at the phenyl ring, which acts as a temporary activating group in a remote position and allows further transformations. The sequential protocol Michael addition/NaBH4 reduction/lactonization allows the synthesis of diastereomerically pure disubstituted lactones in high yield and optical purity." @default.
• W1963599686 created "2016-06-24" @default.
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• W1963599686 date "2010-07-28" @default.
• W1963599686 modified "2023-10-10" @default.
• W1963599686 title "Nitrophenylacetonitriles as Versatile Nucleophiles in Enantioselective Organocatalytic Conjugate Additions" @default.
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• W1963599686 doi "https://doi.org/10.1021/ol101178u" @default.
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• W1963599686 hasPublicationYear "2010" @default.
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