Issue 11, 2011

Synthesis of quaternary stereogenic centres via stereoselective intermolecular Friedel–Crafts reactions

Abstract

Highly stereoselective Friedel–Crafts reactions have been performed using a chiral anthracene template to control the selectivity of the reaction. In the case of additions to fully substituted N-acyliminium ions, competitive elimination and condensation reactions were observed. Retro-Diels–Alder reaction of one of the reaction products led to a precursor that could be used for the construction of pyroglutamic acids bearing quaternary stereogenic centres.

Graphical abstract: Synthesis of quaternary stereogenic centres via stereoselective intermolecular Friedel–Crafts reactions

Supplementary files

Additions and corrections

Article information

Article type
Paper
Submitted
24 Jan 2011
Accepted
22 Mar 2011
First published
20 Apr 2011

Org. Biomol. Chem., 2011,9, 4353-4360

Synthesis of quaternary stereogenic centres via stereoselective intermolecular Friedel–Crafts reactions

J. C. Ball, R. Gleave and S. Jones, Org. Biomol. Chem., 2011, 9, 4353 DOI: 10.1039/C1OB05129F

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