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 22, 2006
Previous Article Next Article

Hosomi–Sakurai reactions of silacyclic allyl silanes

Author affiliations


Substituted silacyclohexenes, generated through silene–diene [4 + 2] cycloaddition reactions, undergo Lewis acid promoted Sakurai type reactions with acetals to afford, following oxidation of the resultant fluorosilane, 1,4-diols with four contiguous chiral centres.

Graphical abstract: Hosomi–Sakurai reactions of silacyclic allyl silanes

Back to tab navigation
Please wait while Download options loads

Supplementary files

Publication details

The article was received on 22 Feb 2006, accepted on 11 Apr 2006 and first published on 02 May 2006

Article type: Communication
DOI: 10.1039/B602642G
Citation: Chem. Commun., 2006, 2385-2387
  •   Request permissions

    Hosomi–Sakurai reactions of silacyclic allyl silanes

    J. D. Sellars, P. G. Steel and M. J. Turner, Chem. Commun., 2006, 2385
    DOI: 10.1039/B602642G

Search articles by author