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Cited by 421

The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

Visible‐Light‐Mediated Generation of Nitrogen‐Centered Radicals: Metal‐Free Hydroimination and Iminohydroxylation Cyclization Reactions

Open access
Davies, Jacob, Booth, Samuel G., Essafi, Stephanie, Dryfe, Robert A. W., Leonori, Daniele·2015·Angewandte Chemie International Edition

Abstract

The formation and use of iminyl radicals in novel and divergent hydroimination and iminohydroxylation cyclization reactions has been accomplished through the design of a new class of reactive O‐aryl oximes. Owing to their low reduction potentials, the inexpensive organic dye eosin Y could be used as the photocatalyst of the organocatalytic hydroimination reaction. Furthermore, reaction conditions for a unique iminohydroxylation were identified; visible‐light‐mediated electron transfer from novel electron donor–acceptor complexes of the oximes and Et 3 N was proposed as a key step of this process.

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Metadata

Authors
Davies, J., Booth, S. G., Essafi, S., Dryfe, R. A. W., & Leonori, D.
Venue
Angewandte Chemie International Edition
Publisher
Wiley
Published
2015-09-28
Volume
54
Issue
47
Pages
14017-14021
ISSN
  • 1433-7851 (ISSN-L)
  • 1521-3773
OpenAlex
W2155753910
Cited by
421
References
2
FWCI
21.13
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Visible‐Light‐Mediated Generation of Nitrogen‐Centered Radicals: Metal‐Free Hydroimination and Iminohydroxylation Cyclization Reactions. https://app.cochat.ai/papers/10.1002/anie.201507641
The paper
Davies, J., Booth, S. G., Essafi, S., Dryfe, R. A. W., & Leonori, D. (2015). Visible‐Light‐Mediated Generation of Nitrogen‐Centered Radicals: Metal‐Free Hydroimination and Iminohydroxylation Cyclization Reactions. Angewandte Chemie International Edition. https://doi.org/10.1002/anie.201507641

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