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Cited by 896

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

Photoorganocatalysis. What for?

Ravelli, Davide, Fagnoni, Maurizio, Albini, Angelo·2013·Chem. Soc. Rev.

Abstract

In the reactions reviewed, an organic molecule under irradiation catalyzes a chemical reaction. The activation is based either on hydrogen or on electron transfer. Commonly used photoorganocatalysts are aromatic ketones, quinones, heterocycles, dyes; intermediates formed are radicals, radical ions and ions from precursors such as alkanes, alkenes, amines, ethers etc. Oxidation (mainly oxygenation) and reduction processes are obtained along with the α-functionalization of amines and ketones, conjugate additions, cycloadditions etc. The key characteristic of the method is the smooth generation of highly reactive intermediates under mild conditions.

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Metadata

Authors
Ravelli, D., Fagnoni, M., & Albini, A.
Venue
Chem. Soc. Rev.
Published
2013
Volume
42
Issue
1
Pages
97-113
ISSN
  • 0306-0012 (ISSN-L)
  • 1460-4744
OpenAlex
W2120612310
Cited by
896
References
1
FWCI
1.90
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Photoorganocatalysis. What for? https://app.cochat.ai/papers/10.1039/c2cs35250h
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Ravelli, D., Fagnoni, M., & Albini, A. (2013). Photoorganocatalysis. What for? Chem. Soc. Rev. https://doi.org/10.1039/c2cs35250h

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

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.