Issue 20, 1998

A novel [2,3] intramolecular rearrangement of N-benzyl-O-allylhydroxylamines

Abstract

A novel [2,3]-sigmatropic rearrangement whereby N-benzyl-O-allylhydroxylamines undergo transformation to the corresponding N-allylhydroxylamines, which can subsequently be reduced to the corresponding allylamines, is described and evidence for the intramolecular nature of this process presented.

Article information

Article type
Paper

Chem. Commun., 1998, 2235-2236

A novel [2,3] intramolecular rearrangement of N-benzyl-O-allylhydroxylamines

S. G. Davies, S. Jones, M. A. Sanz, F. C. Teixeira and J. F. Fox, Chem. Commun., 1998, 2235 DOI: 10.1039/A806200E

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.

Social activity

Spotlight

Advertisements