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- W1520201063 abstract "The reaction of ethylmagnesium bromide, prepared in benzene with one or more molar equivalents of triethylamine, with 2-, 2,4- and 2,4,5-substituted 1,3-dioxolanes has been investigated. Besides β-hydroxyethyl sec-alkyl ethers, the normal products of the ring opening/addition reaction encountered with other Lewis bases, 2-hydroxyethyl enol ethers were formed as products of a ring opening/elimination reaction. Kinetic studies suggest an E1 mechanism for this novel reaction." @default.
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- W1520201063 date "1978-01-01" @default.
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- W1520201063 title "The reaction of Grignard reagents with 1,3-dioxolanes" @default.
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- W1520201063 doi "https://doi.org/10.1016/s0022-328x(00)84088-7" @default.
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