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Efficient Cu‐catalyzed Atom Transfer Radical Addition Reactions of Fluoroalkylsulfonyl Chlorides with Electron‐deficient Alkenes Induced by Visible Light
Open accessAbstract
Fluoroalkylsulfonyl chlorides, R f SO 2 Cl, in which R f=CF 3, C 4 F 9, CF 2 H, CH 2 F, and CH 2 CF 3, are used as a source of fluorinated radicals to add fluoroalkyl groups to electron‐deficient, unsaturated carbonyl compounds. Photochemical conditions, using Cu mediation, are used to produce the respective α‐chloro‐β‐fluoroalkylcarbonyl products in excellent yields through an atom transfer radical addition (ATRA) process. Facile nucleophilic replacement of the α‐chloro substituent is shown to lead to further diverse functionalization of the products.
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Prier, C. K., Rankic, D. A., & MacMillan, D. W. C. (2013) · Chemical Reviews · doi:10.1021/cr300503r · Cited by 9,590
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Contemporary synthetic strategies in organofluorine chemistry
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Metadata
- Authors
- Tang, X., & Dolbier, W. R.
- Venue
- Angewandte Chemie International Edition
- Publisher
- Wiley
- Published
- 2015-02-18
- Volume
- 54
- Issue
- 14
- Pages
- 4246-4249
- ISSN
- 1433-7851 (ISSN-L)
- 1521-3773
- OpenAlex
- W2155016053
- Cited by
- 427
- References
- 1
- FWCI
- 24.72
- Type
- journal article
- Language
- en
- Open access
- bronze
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- Tang, X., & Dolbier, W. R. (2015). Efficient Cu‐catalyzed Atom Transfer Radical Addition Reactions of Fluoroalkylsulfonyl Chlorides with Electron‐deficient Alkenes Induced by Visible Light. Angewandte Chemie International Edition. https://doi.org/10.1002/anie.201412199
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