Secondary Mannich Bases via Trimethylsilyl Trifluoromethanesulphonate Promoted Addition of Silyl Enol Ethers to Schiff Bases

DOI: 10.1039/c39870001053

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 1053 - 1054 (1987)

Update date:2022-08-03

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Authors:

Pilli, R. A.

Russowsky, D.

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Article abstract of DOI:10.1039/c39870001053

A convinient route to N-aryl-β-aminoketones is reported involving addition of silyl enol ethers to Schiff bases activated with 15 molpercent of trimethylsilyl trifluoromethanesulfonate.

Full text of DOI:10.1039/c39870001053

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