Issue 10, 1981

Bis-1,4-dihydronicotinamides. Intramolecular electronic interaction and its consequence in the reduction of a carbonyl substrate in aprotic solvents

Abstract

The reduction of hexachloroacetone in CH2Cl2 or CHCl3 was much enhanced in the presence of 1,6-bis(1-benzyl-1,4-dihydronicotinamido)hexane owing to an intramolecular electronic interaction of charge transfer character.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1981, 444-446

Bis-1,4-dihydronicotinamides. Intramolecular electronic interaction and its consequence in the reduction of a carbonyl substrate in aprotic solvents

Y. Murakami, Y. Aoyama and J. Kikuchi, J. Chem. Soc., Chem. Commun., 1981, 444 DOI: 10.1039/C39810000444

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