Communication
A Novel Bis-Thiourea Organocatalyst for the Asymmetric Aza-Henry Reaction
Article first published online: 24 JUL 2008
DOI: 10.1002/adsc.200800214
Copyright © 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Additional Information
How to Cite
Rampalakos, C. and Wulff, William D. (2008), A Novel Bis-Thiourea Organocatalyst for the Asymmetric Aza-Henry Reaction. Adv. Synth. Catal., 350: 1785–1790. doi: 10.1002/adsc.200800214
Publication History
- Issue published online: 31 JUL 2008
- Article first published online: 24 JUL 2008
- Manuscript Received: 7 APR 2008
Funded by
- NIH. Grant Number: GM 63019
Keywords:
- asymmetric catalysis;
- aza-Henry reaction;
- BINAM;
- nitroalkanes;
- organocatalyst;
- thioureas
Abstract
A novel bis-thiourea/2,2′-diaminobinaphthalene (BINAM)-based catalyst for the asymmetric aza-Henry reaction has been developed. This catalyst promotes the reaction of N-Boc imines with nitroalkanes to afford β-nitroamines with good yields and high enantioselectivities. This catalyst has the advantage that it can be prepared in a single step from commercially available materials. A model is proposed for the catalyst action where both components of the reaction are activated simultaneously by hydrogen bonding. Regardless of the mechanism, the success of the present catalyst demonstrates the potential of bis-thioureas as an interesting class of relatively unexplored catalysts.

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