Successive ring methylation of α-piperidino-oximes by repetitive two-step-reaction

DOI: 10.1002/ardp.19923250606

Source and publish data:

Archiv der Pharmazie p. 335 - 340 (1992)

Update date:2022-07-30

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Authors:

Mohrle Mohrle

Gehlen Gehlen

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Article abstract of DOI:10.1002/ardp.19923250606

Dehydrogenation of α-piperidino-acetophenonoximes with Hg(II)-edta, followed by Grignard reaction, succeeds in the stepwise ring methylation of the piperidine moiety, both E- and Z-isomers retaining their configurations. The kind of ring connection of the

Full text of DOI:10.1002/ardp.19923250606

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