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Cited by 182

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

[2+2] Cycloaddition of 1,3‐Dienes by Visible Light Photocatalysis

Open access
Hurtley, Anna E., Lu, Zhan, Yoon, Tehshik P.·2014·Angewandte Chemie International Edition

Abstract

[2+2] Photocycloadditions of 1,3‐dienes represent a powerful yet synthetically underutilized class of reactions. We report that visible light absorbing transition metal complexes enable the [2+2] cycloaddition of a diverse range of 1,3‐dienes. The ability to use long‐wavelength visible light is attractive because these reaction conditions tolerate the presence of sensitive functional groups that might be readily decomposed by the high‐energy UVC radiation required for direct photoexcitation of 1,3‐dienes. The resulting vinylcyclobutane products are poised for a variety of further diversification reactions, and this method is consequently expected to be powerfully enabling in the synthesis of complex organic targets.

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Metadata

Authors
Hurtley, A. E., Lu, Z., & Yoon, T. P.
Venue
Angewandte Chemie International Edition
Publisher
Wiley
Published
2014-07
Volume
53
Issue
34
Pages
8991-8994
ISSN
  • 1433-7851 (ISSN-L)
  • 1521-3773
OpenAlex
W2146410562
Cited by
182
References
1
FWCI
7.08
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: [2+2] Cycloaddition of 1,3‐Dienes by Visible Light Photocatalysis. https://app.cochat.ai/papers/10.1002/anie.201405359
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Hurtley, A. E., Lu, Z., & Yoon, T. P. (2014). [2+2] Cycloaddition of 1,3‐Dienes by Visible Light Photocatalysis. Angewandte Chemie International Edition. https://doi.org/10.1002/anie.201405359

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

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