The DOI matches its Crossref record.
Visible‐Light‐Induced Photocatalytic Reductive Transformations of Organohalides
Abstract
A photo opportunity: A visible-light-excited iridium catalyst delivers electrons from an amine to an organohalide. The electron transfer then induces reductive scission of the carbon–halogen bond, generating the corresponding alkyl, alkenyl, and aryl radical that can undergo cyclization and hydrodehalogenation reactions.
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Citations
Cited by
Prier, C. K., Rankic, D. A., & MacMillan, D. W. C. (2013) · Chemical Reviews · doi:10.1021/cr300503r · Cited by 9,590
Visible-Light-Driven Reductive Carboarylation of Styrenes with CO 2 and Aryl Halides
Wang, H., Gao, Y., Zhou, C., & Li, G. (2020) · Journal of the American Chemical Society · doi:10.1021/jacs.0c03144 · Cited by 303
Metadata
- Authors
- Kim, H., & Lee, C.
- Venue
- Angewandte Chemie International Edition
- Publisher
- Wiley
- Published
- 2012-11-04
- Volume
- 51
- Issue
- 49
- Pages
- 12303-12306
- ISSN
- 1433-7851 (ISSN-L)
- 1521-3773
- OpenAlex
- W2137921601
- Cited by
- 297
- References
- 0
- FWCI
- 10.79
- Type
- journal article
- Language
- en
- Open access
- closed
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- Kim, H., & Lee, C. (2012). Visible‐Light‐Induced Photocatalytic Reductive Transformations of Organohalides. Angewandte Chemie International Edition. https://doi.org/10.1002/anie.201203599
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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.
