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A Powerful Chiral Counterion Strategy for Asymmetric Transition Metal Catalysis

Open access
Hamilton, Gregory L., Kang, Eun Joo, Mba, Miriam, Toste, F. Dean·2007·Science

Abstract

Traditionally, transition metal–catalyzed enantioselective transformations rely on chiral ligands tightly bound to the metal to induce asymmetric product distributions. Here we report high enantioselectivities conferred by a chiral counterion in a metal-catalyzed reaction. Two different transformations catalyzed by cationic gold(I) complexes generated products in 90 to 99% enantiomeric excess with the use of chiral binaphthol–derived phosphate anions. Furthermore, we show that the chiral counterion can be combined additively with chiral ligands to enable an asymmetric transformation that cannot be achieved by either method alone. This concept of relaying chiral information via an ion pair should be applicable to a vast number of metal-mediated processes.

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Metadata

Authors
Hamilton, G. L., Kang, E. J., Mba, M., & Toste, F. D.
Venue
Science
Published
2007-07-27
Volume
317
Issue
5837
Pages
496-499
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W2057747671
Cited by
909
References
0
FWCI
38.97
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: A Powerful Chiral Counterion Strategy for Asymmetric Transition Metal Catalysis. https://app.cochat.ai/papers/10.1126/science.1145229
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Hamilton, G. L., Kang, E. J., Mba, M., & Toste, F. D. (2007). A Powerful Chiral Counterion Strategy for Asymmetric Transition Metal Catalysis. Science. https://doi.org/10.1126/science.1145229

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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.