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- W2019166111 abstract "The reaction of α-iodoketones with diethylzinc afforded zinc enolates which were converted into the corresponding cyclopropanols in good yields upon treatment with CH2I2 and Et2Zn. The use of α-iodoketone having a carbon-carbon double bond as a substrate proved that cyclopropanation of the enolate moiety proceeded chemoselectively. Cyclopropanation of the zinc enolates derived from α,β-unsaturated ketones via 1,4-addition of organozinc species was also achieved." @default.
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- W2019166111 date "1998-07-01" @default.
- W2019166111 modified "2023-10-09" @default.
- W2019166111 title "Synthesis of cyclopropanols via cyclopropanation of zinc enolates" @default.
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- W2019166111 doi "https://doi.org/10.1016/s0040-4039(98)01036-3" @default.
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