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Palladium-catalyzed oxidative dehydrogenative carbonylation reactions using carbon monoxide and mechanistic overviews
Department of Organic Chemistry, Arrhenius Laboratory, Stockholm University, Stockholm, Sweden.
Department of Organic Chemistry, Arrhenius Laboratory, Stockholm University, Stockholm, Sweden.
Department of Organic Chemistry, Arrhenius Laboratory, Stockholm University, Stockholm, Sweden; Institute of Physical Science and Information Technology, Anhui University, Hefei, China.
Department of Organic Chemistry, Arrhenius Laboratory, Stockholm University, Stockholm, Sweden.
2020 (English)In: Chemical Society Reviews, ISSN 0306-0012, E-ISSN 1460-4744, Vol. 49, p. 341-353Article in journal (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(sp2)-H, and C(sp3)-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
Royal Society of Chemistry, 2020. Vol. 49, p. 341-353
National Category
Natural Sciences
Identifiers
URN: urn:nbn:se:miun:diva-40676DOI: 10.1039/c9cs00397eISI: 000526032600001Scopus ID: 2-s2.0-85078509778OAI: oai:DiVA.org:miun-40676DiVA, id: diva2:1507181
Available from: 2020-12-07 Created: 2020-12-07 Last updated: 2021-05-04Bibliographically approved

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Bäckvall, Jan-Erling

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