Issue 12, 1986

The general quantitative cycloaddition reactions of the dithianitronium cation with olefins: the preparation of 1,3,2-dithiazolium and 1,4-dithia-7-azanorbornylium cations and the crystal and molecular structure of 1,4-dithia-7-azanorbornylium hexafluoroarsenate(V)

Abstract

A number of olefins react quantitatively with S2NAsF6via a concerted symmetry allowed cycloaddition to give 1 : 1 and 2 : 1 stoicheiometric cationic products: the generality of reaction is rationalised and the X-ray crystal structure determination of the 1,4-dithia-7-azanorbornylium cation is reported.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1986, 966-968

The general quantitative cycloaddition reactions of the dithianitronium cation with olefins: the preparation of 1,3,2-dithiazolium and 1,4-dithia-7-azanorbornylium cations and the crystal and molecular structure of 1,4-dithia-7-azanorbornylium hexafluoroarsenate(V)

N. Burford, J. P. Johnson, J. Passmore, M. J. Schriver and P. S. White, J. Chem. Soc., Chem. Commun., 1986, 966 DOI: 10.1039/C39860000966

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