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Synthesis 2022; 54(10): 2330-2339
DOI: 10.1055/a-1739-4793
DOI: 10.1055/a-1739-4793
short review
Photoinduced Organic Reactions by Employing Pyrene Catalysts
This work was supported in part by the Japan Society for the Promotion of Science (JSPS), Grants-in-Aid for Scientific Research (KAKENHI) (Grant Nos. JP 20H04824, and 21H01941), the Yamada Science Foundation, the Sumitomo Foundation, and the Shorai Foundation for Science and Technology.
Abstract
Pyrene is one of the most attractive polycyclic aromatic hydrocarbons (PAHs) in photochemistry. Based on their redox properties, pyrenes have potential as photosensitizers. In this review, we summarize recent developments in pyrene-catalyzed photoinduced organic reactions occurring via energy transfer or single-electron transfer based on the excited state of the pyrene.
1 Introduction
2 Photolysis Involving N–O Bond Cleavage or Decarboxylation
3 (Cyclo)addition Reactions with Styrenes
4 Transformations via Cleavage of C–F, C–I, C–S and C–N Bonds
5 Reactions Based on Sensitization-Initiated Electron Transfer (SenI-ET)
6 Miscellaneous Transformations
7 Conclusion
Key words
pyrene - photoinduced reactions - organic photosensitizer - electron transfer - organic synthesisPublication History
Received: 02 December 2021
Accepted after revision: 13 January 2022
Accepted Manuscript online:
13 January 2022
Article published online:
25 February 2022
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