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- W2950338766 abstract "A new amino alcohol with a chiral cyclopropane backbone has been developed and used in the catalytic asymmetric diethylzinc addition to various types of α-ketoesters. This cyclopropane-based chiral amino alcohol shows moderate enantioselectivity in the addition of organozinc to α-ketoesters. For dimethylzinc addition to α-ketoesters, up to 81% ee are obtained, respectively." @default.
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- W2950338766 date "2009-09-01" @default.
- W2950338766 modified "2023-09-24" @default.
- W2950338766 title "Enantioselective synthesis of quaternary stereogenic centers through catalytic asymmetric addition of dimethylzinc to α-ketoesters with chiral cis-cyclopropane-based amide alcohol as ligand" @default.
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- W2950338766 doi "https://doi.org/10.1016/j.tetasy.2009.07.050" @default.
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