Issue 0, 1966

Cyclic nitrones. Part II. The oxidation of cyclic nitrones by iron(III) chloride

Abstract

2-Unsubstituted 1-pyrroline 1-oxides are rapidly oxidised by iron(III) chloride solutions to yield hydroxamic acids, whilst 2-substituted 1-pyrroline 1-oxides are much more difficult to oxidise. Cyclic hydroxylamines are oxidised as readily as the 1-pyrroline 1-oxides and also yield hydroxamic acids.

Article information

Article type
Paper

J. Chem. Soc. C, 1966, 1477-1479

Cyclic nitrones. Part II. The oxidation of cyclic nitrones by iron(III) chloride

J. F. Elsworth and M. Lamchen, J. Chem. Soc. C, 1966, 1477 DOI: 10.1039/J39660001477

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