ELECTROCHEMICAL AMIDE OXIDATIONS IN THE PRESENCE OF MONOMETHOXYLATED PHENYL RINGS. AN UNEXPECTED RELATIONSHIP BETWEEN THE CHEMOSELECTIVITY OF THE OXIDATION AND THE LOCATION OF THE METHOXY SUBSTITUENT

DOI: 10.1016/S0040-4039(00)72718-3

Source and publish data:

Tetrahedron Letters p. 1213 - 1216 (1989)

Update date:2022-09-26

Topics:

Authors:

Moeller, Kevin D.

Tarazi, Sharif

Marzabadi, Mohammad R.

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Article abstract of DOI:10.1016/S0040-4039(00)72718-3

The chemoselectivity of the electrochemical amide oxidation in the presence of monomethoxylated phenyl rings was examinated.Oxidation of (3-methoxyphenyl)acylpyrrolidine led to exclusive formation of the desired amide oxidation products, while oxidation o

Full text of DOI:10.1016/S0040-4039(00)72718-3

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