Issue 4, 2004

Enantioselective Friedel–Crafts reaction of indoles with arylidene malonates catalyzed by iPr-bisoxazoline–Cu(OTf)2

Abstract

The cheap and simple iPr-bisoxazoline–Cu(OTf)2 proves to be an efficient catalyst in the asymmetric Friedel–Crafts reaction of indole with arylidene malonates. In iBuOH, the S-enantiomer was obtained in up to 97% ee, while the opposite enantiomer was obtained in up to 78% ee in CH2Cl2 or TTCE.

Graphical abstract: Enantioselective Friedel–Crafts reaction of indoles with arylidene malonates catalyzed by iPr-bisoxazoline–Cu(OTf)2

Supplementary files

Article information

Article type
Communication
Submitted
20 Oct 2003
Accepted
15 Dec 2003
First published
19 Jan 2004

Chem. Commun., 2004, 432-433

Enantioselective Friedel–Crafts reaction of indoles with arylidene malonates catalyzed by iPr-bisoxazoline–Cu(OTf)2

J. Zhou and Y. Tang, Chem. Commun., 2004, 432 DOI: 10.1039/B313197A

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