Issue 5, 1998

Electroreductive coupling of vinylpyridines and vinylquinolines: radical anion–substrate cycloaddition?

Abstract

Cathodic reduction of 2- and 4-vinylpyridine and of 2-vinylquinoline gives trans-1,12-di(heteroaryl)cyclobutanes as major products; they arise via radical anion–substrate cycloaddition.

Article information

Article type
Paper

Chem. Commun., 1998, 539-540

Electroreductive coupling of vinylpyridines and vinylquinolines: radical anion–substrate cycloaddition?

R. G. Janssen and M. Motevalli, Chem. Commun., 1998, 539 DOI: 10.1039/A707460C

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.

Social activity

Spotlight

Advertisements