Issue 7, 1974

Regioselective synthesis of Mannich bases from unsymmetrical ketones and immonium salts

Abstract

Isomeric Mannich bases derived from unsymmetrical ketones can be synthesised regioselectively simply by selecting the reaction conditions; reaction of dimethyl(methylene)ammonium trifluoroacetate in trifluoroacetic acid yields the more substituted aminoketone while reaction of di-isopropyl(methylene)ammonium perchlorate in acetonitrile leads to the less substituted aminoketone.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1974, 253b-254

Regioselective synthesis of Mannich bases from unsymmetrical ketones and immonium salts

Y. Jasor, M. Luche, M. Gaudry and A. Marquet, J. Chem. Soc., Chem. Commun., 1974, 253b DOI: 10.1039/C3974000253B

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