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Issue 14, 1987
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Secondary Mannich bases via trimethylsilyl trifluoromethanesulphonate promoted addition of silyl enol ethers to Schiff bases

Abstract

A convenient route to N-aryl-β-aminoketones is reported involving addition of silyl enol ethers to Schiff bases activated with 15 mol % of trimethylsilyl trifluoromethanesulphonate.

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Article information


J. Chem. Soc., Chem. Commun., 1987, 1053-1054
Article type
Paper

Secondary Mannich bases via trimethylsilyl trifluoromethanesulphonate promoted addition of silyl enol ethers to Schiff bases

R. A. Pilli and D. Russowsky, J. Chem. Soc., Chem. Commun., 1987, 1053
DOI: 10.1039/C39870001053

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