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 14, 2004
Previous Article Next Article

The first series of chiral 2,2′:6′,2″-terpyridine tri-N-oxide ligands for Lewis base-catalyzed asymmetric allylation of aldehydes

Author affiliations

Abstract

The first series of chiral 2,2′:6′,2″-terpyridine tri-N-oxide ligands have been developed; They were showed to be active Lewis base-catalysts for asymmetric allylation of aldehydes using allyltrichlorosilane with optimal results at 0 °C for electron-deficient aromatic aldehydes (yields up to 97% and enantioselectivities up to 86% ee).

Graphical abstract: The first series of chiral 2,2′:6′,2″-terpyridine tri-N-oxide ligands for Lewis base-catalyzed asymmetric allylation of aldehydes

Back to tab navigation
Please wait while Download options loads

Publication details

The article was received on 27 May 2004, accepted on 27 May 2004 and first published on 09 Jun 2004


Article type: Communication
DOI: 10.1039/B407933G
Citation: Org. Biomol. Chem., 2004,2, 1967-1969
  •   Request permissions

    The first series of chiral 2,2′:6′,2″-terpyridine tri-N-oxide ligands for Lewis base-catalyzed asymmetric allylation of aldehydes

    W. Wong, C. Lee, H. Leung and H. Kwong, Org. Biomol. Chem., 2004, 2, 1967
    DOI: 10.1039/B407933G

Search articles by author