Issue 14, 1987

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.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1987, 1053-1054

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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