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Cited by 334

The DOI matches its Crossref record; 33 of the 33 references it cites were found in a registry or an index.

Visible-Light-Mediated Synthesis of Amidyl Radicals: Transition-Metal-Free Hydroamination and N-Arylation Reactions

Open access
Davies, Jacob, Svejstrup, Thomas D., Fernandez Reina, Daniel, Sheikh, Nadeem S., Leonori, Daniele·2016·Journal of the American Chemical Society

Abstract

The development of photoredox reactions of aryloxy-amides for the generation of amidyl radicals and their use in hydroamination-cyclization and N-arylation reactions is reported. Owing to the ease of single-electron-transfer reduction of the aryloxy-amides, the organic dye eosin Y was used as the photoredox catalyst, which results in fully transition-metal-free processes. These transformations exhibit a broad scope, are tolerant to several important functionalities, and have been used in the late-stage modification of complex and high-value N-containing molecules.

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Metadata

Authors
Davies, J., Svejstrup, T. D., Fernandez Reina, D., Sheikh, N. S., & Leonori, D.
Venue
Journal of the American Chemical Society
Published
2016-06-27
Volume
138
Issue
26
Pages
8092-8095
ISSN
  • 0002-7863 (ISSN-L)
  • 1520-5126
OpenAlex
W2465356700
Cited by
334
References
33
FWCI
21.23
Type
journal article
Language
en
Open access
hybrid

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CoChat. (2026). Citation check: Visible-Light-Mediated Synthesis of Amidyl Radicals: Transition-Metal-Free Hydroamination and N-Arylation Reactions. https://app.cochat.ai/papers/10.1021/jacs.6b04920
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Davies, J., Svejstrup, T. D., Fernandez Reina, D., Sheikh, N. S., & Leonori, D. (2016). Visible-Light-Mediated Synthesis of Amidyl Radicals: Transition-Metal-Free Hydroamination and N-Arylation Reactions. Journal of the American Chemical Society. https://doi.org/10.1021/jacs.6b04920

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