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Palladium-catalyzed oxidative dehydrogenative carbonylation reactions using carbon monoxide and mechanistic overviews
Stockholm University, Faculty of Science, Department of Organic Chemistry.ORCID iD: 0000-0001-6604-6173
Stockholm University, Faculty of Science, Department of Organic Chemistry.
Stockholm University, Faculty of Science, Department of Organic Chemistry. Anhui University, China.
Stockholm University, Faculty of Science, Department of Organic Chemistry.ORCID iD: 0000-0001-8462-4176
Number of Authors: 42020 (English)In: Chemical Society Reviews, ISSN 0306-0012, E-ISSN 1460-4744, Vol. 49, no 2, p. 341-353Article, review/survey (Refereed) Published
Abstract [en]

Carbon monoxide, which is an abundant and inexpensive carbonyl source, has been widely applied to synthesize carbonyl-containing compounds, for example ketones, esters, and amides. These types of compounds are ubiquitous in natural products, pharmaceuticals, as well as in functional materials. This review focuses on the palladium-catalyzed dehydrogenative C-H/X-H (X = C, N, O) carbonylation transformations under oxidative conditions. The related C-H bonds here include C(sp)-H, C(sp(2))-H, and C(sp(3))-H bonds. From a step- and atom-economy perspective, transition metal-catalyzed oxidative dehydrogenative C-H/X-H carbonylation reactions with CO constitute one of the most efficient strategies for the construction of versatile carbonyl groups, without the requirement of pre-functionalized substrates.

Place, publisher, year, edition, pages
2020. Vol. 49, no 2, p. 341-353
National Category
Chemical Sciences
Identifiers
URN: urn:nbn:se:su:diva-181991DOI: 10.1039/c9cs00397eISI: 000526032600001PubMedID: 31850426OAI: oai:DiVA.org:su-181991DiVA, id: diva2:1432569
Available from: 2020-05-27 Created: 2020-05-27 Last updated: 2022-03-23Bibliographically approved

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Zhu, CanLiu, JieLi, Man-BoBäckvall, Jan-E.

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