Issue 8, 2011

Dinuclear zinc catalyzed asymmetric Friedel–Crafts amidoalkylation of indoles with aryl aldimines

Abstract

The asymmetric Friedel–Crafts amidoalkylation of indoles with aryl aldimines could be efficiently catalyzed by Trost's bis-ProPhenol dinuclear zinc complexes to attain 3-indolyl methanamine derivatives in good to excellent yields (85–98%) with moderate to high enantiomeric ratios (from 70 : 30 up to 95 : 5 er). Remarkably, this approach provides efficient access to enantiomerically enriched 3-indolyl methanamines, which avoids the formation of the undesirable bis- and tris(indolyl)methanes (BIMs and TIMs) byproduct.

Graphical abstract: Dinuclear zinc catalyzed asymmetric Friedel–Crafts amidoalkylation of indoles with aryl aldimines

Supplementary files

Article information

Article type
Communication
Submitted
18 Dec 2010
Accepted
09 Feb 2011
First published
14 Feb 2011

Org. Biomol. Chem., 2011,9, 2614-2617

Dinuclear zinc catalyzed asymmetric Friedel–Crafts amidoalkylation of indoles with aryl aldimines

B. Wang, N. Li, J. Zhang, G. Liu, T. Liu, Q. Shen and X. Wang, Org. Biomol. Chem., 2011, 9, 2614 DOI: 10.1039/C0OB01200A

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