Issue 0, 1967

Nitramines. Part IV. Preparation and nitrolysis of the condensation products of ethylenedinitramine with formaldehyde and some diamines

Abstract

Bicyclic nitramines obtained by Mannich condensations of ethylenedinitramine with formaldehyde and primary diamines have been converted into linear diacetates by nitrolysis in acetic anhydride. Further reactions of the diacetates with nitric acid are described.

Article information

Article type
Paper

J. Chem. Soc. C, 1967, 562-565

Nitramines. Part IV. Preparation and nitrolysis of the condensation products of ethylenedinitramine with formaldehyde and some diamines

J. A. Bell and I. Dunstan, J. Chem. Soc. C, 1967, 562 DOI: 10.1039/J39670000562

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