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Cited by 551

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Three‐component Oxytrifluoromethylation of Alkenes: Highly Efficient and Regioselective Difunctionalization of CC Bonds Mediated by Photoredox Catalysts

Yasu, Yusuke, Koike, Takashi, Akita, Munetaka·2012·Angewandte Chemie International Edition

Abstract

Here comes the sun: A facile vicinal difunctionalization of alkenes, oxytrifluoromethylation, was established by visible-light-driven photoredox catalysis. Judicious choice of the CF3 source is key. Nucleophiles such as water, alcohols, and carboxylic acids can be used in this highly efficient (2–4 h) and regioselective (100 %) transformation using light-emitting diode (LED) lamps and natural sunlight. SET=single-electron transfer.

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Metadata

Authors
Yasu, Y., Koike, T., & Akita, M.
Venue
Angewandte Chemie International Edition
Publisher
Wiley
Published
2012-08-31
Volume
51
Issue
38
Pages
9567-9571
ISSN
  • 1433-7851 (ISSN-L)
  • 1521-3773
OpenAlex
W2105276976
Cited by
551
References
0
FWCI
32.52
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Three‐component Oxytrifluoromethylation of Alkenes: Highly Efficient and Regioselective Difunctionalization of CC Bonds Mediated by Photoredox Catalysts. https://app.cochat.ai/papers/10.1002/anie.201205071
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Yasu, Y., Koike, T., & Akita, M. (2012). Three‐component Oxytrifluoromethylation of Alkenes: Highly Efficient and Regioselective Difunctionalization of CC Bonds Mediated by Photoredox Catalysts. Angewandte Chemie International Edition. https://doi.org/10.1002/anie.201205071

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