Issue 11, 1997

Oxidation of Isothiocyanates to Isocyanates using Dimethyldioxirane; Relevance to Biological Activity of Isothiocyanates†

Abstract

The reaction of organic isothiocyanates with dimethyldioxirane in acetone produces isocyanates in good yields, trapped out as the ureas by reaction with isopropylamine.

Article information

Article type
Paper

J. Chem. Res. (S), 1997, 410-411

Oxidation of Isothiocyanates to Isocyanates using Dimethyldioxirane; Relevance to Biological Activity of Isothiocyanates†

N. E. Davidson and N. P. Botting, J. Chem. Res. (S), 1997, 410 DOI: 10.1039/A704356B

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