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- W2032131687 abstract "Silyl enolates that were generated from α-allyloxy esters afforded the corresponding [2,3]-Wittig rearrangement products in moderate to good yields on treatment with a catalytic amount of Lewis base such as tetrabutylammonium acetate or tetrabutylammonium 4-methoxybenzoate in DMF at room temperature." @default.
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- W2032131687 date "2005-08-01" @default.
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- W2032131687 title "Ammonium Carboxylate-catalyzed [2,3]-Wittig Rearrangement of Silyl Enolates Generated from α-Allyloxy Esters" @default.
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