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Theoretical Study of the Mechanism of Hantzsch Ester Hydrogenation of Imines Catalyzed by Chiral BINOL-Phosphoric Acids
Abstract
The mechanism of the Hantzsch ester hydrogenation of imines catalyzed by chiral BINOL-phosphoric acid has been investigated using DFT methods. Despite the importance of this reaction, there are a number of possible detailed mechanisms, and the preferred pathway has not been firmly established. Our calculations show that the catalyst not only activates the imine group for the reaction by acting as a Brønsted acid but also establishes an interaction with the Hantzsch ester that can lead to an explanation for the enantioselectivity.
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Cites
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Metadata
- Authors
- Simón, L., & Goodman, J. M.
- Venue
- Journal of the American Chemical Society
- Publisher
- American Chemical Society (ACS)
- Published
- 2008-06-11
- Volume
- 130
- Issue
- 27
- Pages
- 8741-8747
- ISSN
- 0002-7863 (ISSN-L)
- 1520-5126
- OpenAlex
- W2079821320
- Cited by
- 295
- References
- 24
- FWCI
- 11.72
- Type
- journal article
- Language
- en
- Open access
- closed
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- Simón, L., & Goodman, J. M. (2008). Theoretical Study of the Mechanism of Hantzsch Ester Hydrogenation of Imines Catalyzed by Chiral BINOL-Phosphoric Acids. Journal of the American Chemical Society. https://doi.org/10.1021/ja800793t
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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