Acyl radicals were smoothly generated from acylsilanes under photoredoxcatalyzed conditions. These radicals were formed upon ultraviolet B (UV-B), solar, or visible light irradiation by using decatungstate and acridinium salts as photocatalysts. Acylation of Michael acceptors and a few styrenes resulted in a smooth preparation of unsymmetrical ketones in yields up to 89%.
Acyl Radicals from Acylsilanes: Photoredox Catalyzed Synthesis of Unsymmetrical Ketones / Capaldo, L; Riccardi, R.; Ravelli, D.; Fagnoni, M.. - In: ACS CATALYSIS. - ISSN 2155-5435. - 8:(2018), pp. 304-309. [10.1021/acscatal.7b03719]
Acyl Radicals from Acylsilanes: Photoredox Catalyzed Synthesis of Unsymmetrical Ketones
Capaldo L;Ravelli D.;
2018-01-01
Abstract
Acyl radicals were smoothly generated from acylsilanes under photoredoxcatalyzed conditions. These radicals were formed upon ultraviolet B (UV-B), solar, or visible light irradiation by using decatungstate and acridinium salts as photocatalysts. Acylation of Michael acceptors and a few styrenes resulted in a smooth preparation of unsymmetrical ketones in yields up to 89%.File in questo prodotto:
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