The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Photoredox activation and anion binding catalysis in the dual catalytic enantioselective synthesis of β-amino esters
Open accessAbstract
The enantioselective oxidative C-H functionalization of tetrahydroisoquinoline derivatives is achieved through the merger of photoredox and asymmetric anion-binding catalysis. This combination of two distinct catalysis concepts introduces a potentially general approach to asymmetric transformations in oxidative photocatalysis.
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Citations
Cites
Prier, C. K., Rankic, D. A., & MacMillan, D. W. C. (2013) · Chemical Reviews · doi:10.1021/cr300503r · Cited by 9,590
Cited by
Tay, N. E. S., Lehnherr, D., & Rovis, T. (2022) · Chemical Reviews · doi:10.1021/acs.chemrev.1c00384 · Cited by 518
Metadata
- Authors
- Bergonzini, G., Schindler, C. S., Wallentin, C.-J., Jacobsen, E. N., & Stephenson, C. R. J.
- Venue
- Chem. Sci.
- Publisher
- Royal Society of Chemistry (RSC)
- Published
- 2014
- Volume
- 5
- Issue
- 1
- Pages
- 112-116
- ISSN
- 2041-6520 (ISSN-L)
- 2041-6539
- OpenAlex
- W1966519091
- Cited by
- 277
- References
- 1
- FWCI
- 16.87
- Type
- journal article
- Language
- en
- Open access
- green
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- The paper
- Bergonzini, G., Schindler, C. S., Wallentin, C.-J., Jacobsen, E. N., & Stephenson, C. R. J. (2014). Photoredox activation and anion binding catalysis in the dual catalytic enantioselective synthesis of β-amino esters. Chem. Sci. https://doi.org/10.1039/c3sc52265b
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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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