Issue 24, 1987

The in situ generation of thiazyl trichloride: a synthon for C–N–S heterocycles

Abstract

The novel reagent NSCl3 is readily generated by treatment of (NSCl)3 with an excess of SO2Cl2; the reactions of NSCl3 with methacrylonitirle or thioacetamide produce 4-cyanosiothiazole or 5-methyl-1,3,2,4-dithiazolium chloride, respectively, in good yields.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1987, 1889-1890

The in situ generation of thiazyl trichloride: a synthon for C–N–S heterocycles

A. Apblett and T. Chivers, J. Chem. Soc., Chem. Commun., 1987, 1889 DOI: 10.1039/C39870001889

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