The DOI matches its Crossref record.
Anti-Markovnikov Hydroamination of Alkenes Catalyzed by an Organic Photoredox System
Open accessAbstract
Herein we report a metal-free method for the direct anti-Markovnikov hydroamination of unsaturated amines. Irradiation of the amine substrates with visible light in the presence of catalytic quantities of easily synthesized 9-mesityl-10-methylacridinium tetrafluoroborate and thiophenol as a hydrogen-atom donor furnished the nitrogen-containing heterocycles with complete regiocontrol. Two examples of intermolecular anti-Markovnikov alkene hydroamination are also disclosed.
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Fernández-García, E. (2014) · Food & Function · doi:10.1039/c4fo00280f · Cited by 108
Metadata
- Authors
- Nguyen, T. M., & Nicewicz, D. A.
- Venue
- Journal of the American Chemical Society
- Publisher
- American Chemical Society (ACS)
- Published
- 2013-06-19
- Volume
- 135
- Issue
- 26
- Pages
- 9588-9591
- ISSN
- 0002-7863 (ISSN-L)
- 1520-5126
- OpenAlex
- W2074545790
- Cited by
- 331
- References
- 0
- FWCI
- 14.01
- Type
- journal article
- Language
- en
- Open access
- green
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- CoChat. (2026). Citation check: Anti-Markovnikov Hydroamination of Alkenes Catalyzed by an Organic Photoredox System. https://app.cochat.ai/papers/10.1021/ja4031616
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- Nguyen, T. M., & Nicewicz, D. A. (2013). Anti-Markovnikov Hydroamination of Alkenes Catalyzed by an Organic Photoredox System. Journal of the American Chemical Society. https://doi.org/10.1021/ja4031616
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
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.
