We thank NIGMS for generous support of this research (GM 36700 to K.N.H. and GM 72586 to T.R.). T.R. thanks Amgen and Roche for unrestricted support. E.L.N. is grateful to the National Institutes of Health Chemistry-Biology Interface Training Program Grant (T32M008496). K.N.H. is grateful to the National Science Foundation (CHE-0548209) for financial support, to the UCLA Academic Technology Services (ATS) Hoffman2 and IDRE clusters for computational resources, and for the TeraGrid resources provided by NCSA (CHE-0400414).
Catalytic Asymmetric Intermolecular Stetter Reactions of Enolizable Aldehydes with Nitrostyrenes: Computational Study Provides Insight into the Success of the Catalyst†
Article first published online: 26 JAN 2012
Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Angewandte Chemie International Edition
Volume 51, Issue 10, pages 2391–2394, March 5, 2012
How to Cite
DiRocco, D. A., Noey, E. L., Houk, K. N. and Rovis, T. (2012), Catalytic Asymmetric Intermolecular Stetter Reactions of Enolizable Aldehydes with Nitrostyrenes: Computational Study Provides Insight into the Success of the Catalyst. Angew. Chem. Int. Ed., 51: 2391–2394. doi: 10.1002/anie.201107597
- Issue published online: 1 MAR 2012
- Article first published online: 26 JAN 2012
- Manuscript Revised: 20 DEC 2011
- Manuscript Received: 27 OCT 2011
- NIGMS. Grant Numbers: GM 36700, GM 72586
- National Institutes of Health Chemistry-Biology Interface Training Program Grant. Grant Number: T32M008496
- National Science Foundation. Grant Numbers: CHE-0548209, CHE-0400414
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