Jump to main content
Jump to site search
PLANNED MAINTENANCE Close the message box

Scheduled maintenance upgrade on Thursday 4th of May 2017 from 8.00am to 9.00am (BST).

During this time our websites will be offline temporarily. If you have any questions please use the feedback button on this page. We apologise for any inconvenience this might cause and thank you for your patience.


Issue 7, 2005
Previous Article Next Article

A general method for making bicyclic compounds with nitrogen at a bridgehead—application to the halichlorine spiro subunit

Author affiliations

Abstract

N-Protected β-amino aldehydes having the nitrogen in a ring are easily converted into Morita–Baylis–Hillman adducts; O-acetylation and N-deprotection result in spontaneous cyclization to bicyclic structures having nitrogen at a bridgehead.

Graphical abstract: A general method for making bicyclic compounds with nitrogen at a bridgehead—application to the halichlorine spiro subunit

Back to tab navigation
Please wait while Download options loads

Supplementary files

Publication details

The article was received on 26 Aug 2004, accepted on 07 Oct 2004 and first published on 23 Dec 2004


Article type: Communication
DOI: 10.1039/B413481H
Citation: Chem. Commun., 2005, 906-908
  •   Request permissions

    A general method for making bicyclic compounds with nitrogen at a bridgehead—application to the halichlorine spiro subunit

    D. L. J. Clive, M. Yu and Z. Li, Chem. Commun., 2005, 906
    DOI: 10.1039/B413481H

Search articles by author