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Cited by 295

The DOI matches its Crossref record; 24 of the 24 references it cites were found in a registry or an index.

Theoretical Study of the Mechanism of Hantzsch Ester Hydrogenation of Imines Catalyzed by Chiral BINOL-Phosphoric Acids

Simón, Luis, Goodman, Jonathan M.·2008·Journal of the American Chemical Society

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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Metadata

Authors
Simón, L., & Goodman, J. M.
Venue
Journal of the American Chemical Society
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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CoChat. (2026). Citation check: Theoretical Study of the Mechanism of Hantzsch Ester Hydrogenation of Imines Catalyzed by Chiral BINOL-Phosphoric Acids. https://app.cochat.ai/papers/10.1021/ja800793t
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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).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.