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Pd(II)-Catalyzed C-H Acylation of (Hetero)arenes. Recent Advances

dc.contributor.authorSantiago Alvarez, Carlos
dc.contributor.authorSotomayor Anduiza, María Nuria
dc.contributor.authorLete Expósito, María Esther
dc.date.accessioned2020-08-03T11:56:49Z
dc.date.available2020-08-03T11:56:49Z
dc.date.issued2020-07-16
dc.identifier.citationMolecules 25(14) : (2020) // Article ID 3247es_ES
dc.identifier.issn1420-3049
dc.identifier.urihttp://hdl.handle.net/10810/45827
dc.description.abstractDi(hetero)aryl ketones are important motifs present in natural products, pharmaceuticals or agrochemicals. In recent years, Pd(II)-catalyzed acylation of (hetero)arenes in the presence of an oxidant has emerged as a catalytic alternative to classical acylation methods, reducing the production of toxic metal waste. Different directing groups and acyl sources are being studied for this purpose, although further development is required to face mainly selectivity problems in order to be applied in the synthesis of more complex molecules. Selected recent developments and applications are covered in this review.es_ES
dc.description.sponsorshipThis work is supported by Ministerio de Economía y Competitividad (CTQ2016-74881-P), Ministerio de Ciencia e Innovación (PID2019-104148GB-I00) and Gobierno Vasco (IT1045-16).es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/CTQ2016-74881-Pes_ES
dc.relationinfo:eu-repo/grantAgreement/MCIU/PID2019-104148GB-I00es_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/
dc.subjectC-H activationes_ES
dc.subjectacylationes_ES
dc.subjectpalladiumes_ES
dc.subjectareneses_ES
dc.subjectheteroareneses_ES
dc.titlePd(II)-Catalyzed C-H Acylation of (Hetero)arenes. Recent Advanceses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.date.updated2020-07-24T13:39:25Z
dc.rights.holder© 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).es_ES
dc.relation.publisherversionhttps://www.mdpi.com/1420-3049/25/14/3247es_ES
dc.identifier.doi10.3390/molecules25143247
dc.departamentoesQuímica orgánica II
dc.departamentoeuKimika organikoa II


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© 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
Except where otherwise noted, this item's license is described as © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).