Record link: 
http://hdl.handle.net/20.500.12708/139180
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Title: 
Photocatalyst-free hydroacylations of electron-poor alkenes and enones under visible-light irradiation
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Citation: 
Pálvölgyi, Á. M., Ehrschwendtner, F., Schnürch, M., & Bica-Schröder, K. (2022). Photocatalyst-free hydroacylations of electron-poor alkenes and enones under visible-light irradiation. Organic and Biomolecular Chemistry, 20(36), 7245–7249. https://doi.org/10.1039/d2ob01364a
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Publisher DOI: 
10.1039/d2ob01364a
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Publication Type: 
Article - Original Research Article
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Language: 
English
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Authors: 
Pálvölgyi, Ádám Márk 
Ehrschwendtner, Florian 
Schnürch, Michael 
Bica-Schröder, Katharina 
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Organisational Unit: 
E163 - Institut für Angewandte Synthesechemie 
E163-03-5 - Forschungsgruppe Nachhaltige organische Synthese und Katalyse 
E163-03-4 - Forschungsgruppe Bioorganische Synthesechemie 
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Journal: 
Organic and Biomolecular Chemistry 
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ISSN: 
1477-0520
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Date (published): 
21-Sep-2022
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Number of Pages: 
5
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Publisher: 
ROYAL SOC CHEMISTRY
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Peer reviewed: 
Yes
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Keywords: 
Catalysis; Electrons; Esters; Free Radicals; Alkenes; Photochemical Processes
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Abstract: 
Herein we present a photocatalyst- and additive-free radical hydroacylation of electron-poor double bonds under mild reaction conditions. Using 4-acyl-Hantzsch ester radical reservoirs, various Michael acceptors, enones and para-quinone methide substrates could be used. The protocol enabled further derivatizations and it could also be extended to a few unactivated alkenes. Moreover, the nature of the radical process was also investigated.
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Project (external): 
European Union's Horizon 2020
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Project ID: 
D163035-1002
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Research Areas: 
Biological and Bioactive Materials: 100%
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Science Branch: 
1040 - Chemie: 60%
2040 - Chemische Verfahrenstechnik: 20%
3012 - Pharmazie, Pharmakologie, Toxikologie: 20%
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