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- W2006366185 abstract "2,2-Dimethoxyethyl 2-alkenoates are easily transformed into 2-(1-alkenyl)-1,3-dioxolan-2-ylium cations in situ on the action of titanium tetrachloride, which react with enamines to predominantly give syn Michael adducts in good yields. This is the first example of such a high syn-selectivity for the Michael reaction of α,β-unsaturated ester derivatives with ketone enolate equivalents." @default.
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- W2006366185 date "1991-01-01" @default.
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- W2006366185 title "The highly syn-selective Michael reaction of enamines with 2-(1-alkenyl)-1,3-dioxolan-2-ylium cations generated from 2,2-dimethoxyethyl 2-alkenoates in situ" @default.
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- W2006366185 doi "https://doi.org/10.1016/s0040-4020(01)80900-5" @default.
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