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Organophotoredox 1,6-Addition of 3,4-Dihydroquinoxalin-2-ones to para-Quinone Methides Using Visible Light.

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Organophotoredox 1,6-Addition of 3,4-Dihydroquinoxalin-2-ones to para-Quinone Methides Using Visible Light.

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dc.contributor.author	Rostoll Berenguer, Jaume
dc.contributor.author	García García, Victor
dc.contributor.author	Blay Llinares, Gonzalo
dc.contributor.author	Pedro, José Ramón
dc.contributor.author	Vila Descals, Carlos
dc.date.accessioned	2023-06-22T07:17:22Z
dc.date.available	2023-06-22T07:17:22Z
dc.date.issued	2023
dc.identifier.citation	Rostoll Berenguer, Jaume García García, Victor Blay Llinares, Gonzalo Pedro, José Ramón Vila Descals, Carlos 2023 Organophotoredox 1,6-Addition of 3,4-Dihydroquinoxalin-2-ones to para-Quinone Methides Using Visible Light. ACS Organic & Inorganic Au 3 3 130 135
dc.identifier.uri	https://hdl.handle.net/10550/88432
dc.description.abstract	An organophotoredox 1,6-radical addition of 3,4-dihidroquinoxalin-2-ones to para-quinone methides catalyzed by Fukuzumi's photocatalyst is described under the irradiation of a HP Single LED (455 nm). The corresponding 1,1-diaryl compounds bearing a dihydroquinoxalin-2-one moiety (20 examples) are obtained with good to excellent yields under mild reaction conditions. Several experiments have been carried out in order to propose a reaction mechanism.
dc.language.iso	eng
dc.relation.ispartof	ACS Organic & Inorganic Au, 2023, vol. 3, num. 3, p. 130-135
dc.subject	Química
dc.title	Organophotoredox 1,6-Addition of 3,4-Dihydroquinoxalin-2-ones to para-Quinone Methides Using Visible Light.
dc.type	journal article
dc.date.updated	2023-06-22T07:17:22Z
dc.identifier.doi	10.1021/acsorginorgau.2c00064
dc.identifier.idgrec	160458
dc.rights.accessRights	open access