Jump to main content
Jump to site search

Issue 27, 2012
Previous Article Next Article

Strategies for the enantioselective synthesis of spirooxindoles

Author affiliations

Abstract

Oxindoles and spirooxindoles are important synthetic targets that are often considered to be prevalidated with respect to their biological activity and applications for pharmaceutical lead discovery. This review features efficient strategies for the enantioselective synthesis of spirocyclic oxindoles, focusing on reports in 2010 and 2011. Although enantioselective synthesis remains an ongoing challenge, exciting recent advances in this area feature spirooxindoles with greater complexity, up to eight stereogenic centers, more practical synthetic methods, and new catalytic activation strategies. Developments in catalyst systems and reaction conditions have shown that many reactions can be optimized to control selectivity and provide access to isomeric products, which are important for biological testing. This review is organized based on two primary disconnection strategies, and then further subdivided into the type and ring size of the spirocycle that is generated. Strategies are also compared for the synthesis of non-spirocyclic 3,3′-disubstituted oxindoles.

Graphical abstract: Strategies for the enantioselective synthesis of spirooxindoles

Back to tab navigation

Article information


Submitted
25 Jan 2012
Accepted
11 Apr 2012
First published
16 Apr 2012

Org. Biomol. Chem., 2012,10, 5165-5181
Article type
Perspective

Strategies for the enantioselective synthesis of spirooxindoles

N. R. Ball-Jones, J. J. Badillo and A. K. Franz, Org. Biomol. Chem., 2012, 10, 5165
DOI: 10.1039/C2OB25184A

Social activity

Search articles by author

Spotlight

Advertisements