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 54, 2013
Previous Article Next Article

Organocatalytic asymmetric desymmetrization: efficient construction of spirocyclic oxindoles bearing a unique all-carbon quaternary stereogenic center via sulfa-Michael addition

Author affiliations

Abstract

An unprecedented enantioselective desymmetrization of spiro cyclohexadienone oxindoles has been developed successfully via organocatalyzed asymmetric SMA, which provides facile access to spirocyclic oxindoles bearing a unique all-carbon quaternary stereogenic center with excellent levels of stereoselectivity.

Graphical abstract: Organocatalytic asymmetric desymmetrization: efficient construction of spirocyclic oxindoles bearing a unique all-carbon quaternary stereogenic center via sulfa-Michael addition

Back to tab navigation
Please wait while Download options loads

Supplementary files

Publication details

The article was received on 09 Apr 2013, accepted on 15 May 2013 and first published on 16 May 2013


Article type: Communication
DOI: 10.1039/C3CC42587H
Citation: Chem. Commun., 2013,49, 6078-6080
  •   Request permissions

    Organocatalytic asymmetric desymmetrization: efficient construction of spirocyclic oxindoles bearing a unique all-carbon quaternary stereogenic center via sulfa-Michael addition

    L. Yao, K. Liu, H. Tao, G. Qiu, X. Zhou and C. Wang, Chem. Commun., 2013, 49, 6078
    DOI: 10.1039/C3CC42587H

Search articles by author