Issue 14, 1973

Electrochemical acylation of aromatic compounds

Abstract

Acylation of a range of aromatic compounds has been effected by the in situ generation of an energetic acylating species during the anodic oxidation at vitreous carbon of 2,3,5,6-tetramethoxyquinol diacetate in trifluoroacetic acid solution.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1973, 473-474

Electrochemical acylation of aromatic compounds

J. H. P. Utley and G. B. Yates, J. Chem. Soc., Chem. Commun., 1973, 473 DOI: 10.1039/C39730000473

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements