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Electrosynthetic C−O Bond Activation in Alcohols and Alcohol Derivatives
KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Kemi, Organisk kemi.
KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Kemi, Organisk kemi.ORCID-id: 0000-0002-7249-7437
KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Kemi, Organisk kemi.ORCID-id: 0000-0002-6089-5454
KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Kemi, Organisk kemi.ORCID-id: 0000-0002-4704-1892
2023 (engelsk)Inngår i: Angewandte Chemie International Edition, ISSN 1433-7851, E-ISSN 1521-3773, Vol. 62, nr 4, artikkel-id e202211952Artikkel, forskningsoversikt (Fagfellevurdert) Published
Abstract [en]

Alcohols and their derivatives are ubiquitous and versatile motifs in organic synthesis. Deoxygenative transformations of these compounds are often challenging due to the thermodynamic penalty associated with the cleavage of the C−O bond. However, electrochemically driven redox events have been shown to facilitate the C−O bond cleavage in alcohols and their derivatives either through direct electron transfer or through the use of electron transfer mediators and electroactive catalysts. Herein, a comprehensive overview of preparative electrochemically mediated protocols for C−O bond activation and functionalization is detailed, including direct and indirect electrosynthetic methods, as well as photoelectrochemical strategies.

sted, utgiver, år, opplag, sider
Wiley , 2023. Vol. 62, nr 4, artikkel-id e202211952
Emneord [en]
Alcohol, Cathodic Reduction, C−O Bond Activation, Deoxygenative, Electrosynthesis
HSV kategori
Identifikatorer
URN: urn:nbn:se:kth:diva-329096DOI: 10.1002/anie.202211952ISI: 000897611400001PubMedID: 36278406Scopus ID: 2-s2.0-85143435718OAI: oai:DiVA.org:kth-329096DiVA, id: diva2:1768458
Merknad

QC 20230615

Tilgjengelig fra: 2023-06-15 Laget: 2023-06-15 Sist oppdatert: 2023-06-15bibliografisk kontrollert

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Villo, PiretShatskiy, AndreyKärkäs, Markus D.Lundberg, Helena

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