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Cited by 269

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Photoredox Imino Functionalizations of Olefins

Open access
Davies, Jacob, Sheikh, Nadeem S., Leonori, Daniele·2017·Angewandte Chemie International Edition

Abstract

Shown herein is that polyfunctionalized nitrogen heterocycles can be easily prepared by a visible‐light‐mediated radical cascade process. This divergent strategy features the oxidative generation of iminyl radicals and subsequent cyclization/radical trapping, which allows the effective construction of highly functionalized heterocycles. The reactions proceed efficiently at room temperature, utilize an organic photocatalyst, use simple and readily available materials, and generate, in a single step, valuable building blocks that would be difficult to prepare by other methods.

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Metadata

Authors
Davies, J., Sheikh, N. S., & Leonori, D.
Venue
Angewandte Chemie International Edition
Publisher
Wiley
Published
2017-09-22
Volume
56
Issue
43
Pages
13361-13365
ISSN
  • 1433-7851 (ISSN-L)
  • 1521-3773
OpenAlex
W2753297060
Cited by
269
References
1
FWCI
13.49
Type
journal article
Language
en
Open access
hybrid

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CoChat. (2026). Citation check: Photoredox Imino Functionalizations of Olefins. https://app.cochat.ai/papers/10.1002/anie.201708497
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Davies, J., Sheikh, N. S., & Leonori, D. (2017). Photoredox Imino Functionalizations of Olefins. Angewandte Chemie International Edition. https://doi.org/10.1002/anie.201708497

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.