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 ...