Issue 1, 1982
From the journal:

Journal of the Chemical Society, Perkin Transactions 2

Compounds with bridgehead nitrogen. Part 41. The reaction between trans-2-aminocycloalkanols and formaldehyde

Peter M. R. Barkworth  and  Trevor A. Crabb  

Abstract

trans-2-Aminocyclopentanol and trans-2-aminocyclohexanol condense with formaldehyde to give single isomers of NN′-methanoperhydrocycloalkano[d,i][1,6,3,8]dioxadiazecines whereas trans-2-aminocycloheptanol and trans-2-aminocyclo-octanol give 1 : 1 mixtures of two isomeric bis(perhydrocycloaikeno-oxazol-3-yl)methanes. The formation of the two types of dimer is explained in terms of differences in ring fusion strain.

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/P29820000091
Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1982, 91-94

Permissions

Request permissions

Compounds with bridgehead nitrogen. Part 41. The reaction between trans-2-aminocycloalkanols and formaldehyde

P. M. R. Barkworth and T. A. Crabb, J. Chem. Soc., Perkin Trans. 2, 1982, 91 DOI: 10.1039/P29820000091

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