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

Scheduled maintenance work on Wednesday 22nd May 2019 from 11:00 AM to 1:00 PM (GMT).

During this time our website performance may be temporarily affected. We apologise for any inconvenience this might cause and thank you for your patience.


Issue 23, 2008
Previous Article Next Article

Directed epoxidation of cyclohexa-1,4-dienes–stereoselective formation of up to six contiguous stereogenic centres

Author affiliations

Abstract

Epoxidation/cyclisation of cyclohexa-1,4-dienes containing pendant hydroxyl groups provides stereocontrolled access to highly-functionalised reduced benzol[b]furan derivatives.

Graphical abstract: Directed epoxidation of cyclohexa-1,4-dienes–stereoselective formation of up to six contiguous stereogenic centres

Back to tab navigation

Supplementary files

Publication details

The article was received on 13 Aug 2008, accepted on 29 Aug 2008 and first published on 20 Oct 2008


Article type: Paper
DOI: 10.1039/B814131M
Org. Biomol. Chem., 2008,6, 4426-4434

  •   Request permissions

    Directed epoxidation of cyclohexa-1,4-dienes–stereoselective formation of up to six contiguous stereogenic centres

    M. Butters, D. J. Beetstra, M. C. Elliott, J. Hill-Cousins and B. M. Kariuki, Org. Biomol. Chem., 2008, 6, 4426
    DOI: 10.1039/B814131M

Search articles by author

Spotlight

Advertisements