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Cited by 200

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Cooperative Light‐Activated Iodine and Photoredox Catalysis for the Amination of C−H Bonds

Open access
Becker, Peter, Duhamel, Thomas, Stein, Christopher J., Reiher, Markus, Muñiz, Kilian·2017·Angewandte Chemie International Edition

Abstract

An unprecedented method that makes use of the cooperative interplay between molecular iodine and photoredox catalysis has been developed for dual light‐activated intramolecular benzylic C−H amination. Iodine serves as the catalyst for the formation of a new C−N bond by activating a remote C −H bond (1,5‐HAT process) under visible‐light irradiation while the organic photoredox catalyst TPT effects the reoxidation of the molecular iodine catalyst. To explain the compatibility of the two involved photochemical steps, the key N−I bond activation was elucidated by computational methods. The new cooperative catalysis has important implications for the combination of non‐metallic main‐group catalysis with photocatalysis.

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Metadata

Authors
Becker, P., Duhamel, T., Stein, C. J., Reiher, M., & Muñiz, K.
Venue
Angewandte Chemie International Edition
Publisher
Wiley
Published
2017-06
Volume
56
Issue
27
Pages
8004-8008
ISSN
  • 1433-7851 (ISSN-L)
  • 1521-3773
OpenAlex
W2620813024
Cited by
200
References
1
FWCI
13.05
Type
journal article
Language
en
Open access
hybrid

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CoChat. (2026). Citation check: Cooperative Light‐Activated Iodine and Photoredox Catalysis for the Amination of C−H Bonds. https://app.cochat.ai/papers/10.1002/anie.201703611
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Becker, P., Duhamel, T., Stein, C. J., Reiher, M., & Muñiz, K. (2017). Cooperative Light‐Activated Iodine and Photoredox Catalysis for the Amination of C−H Bonds. Angewandte Chemie International Edition. https://doi.org/10.1002/anie.201703611

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