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Highly Diastereoselective Palladium-Catalyzed Oxidative Cascade Carbonylative Carbocyclization of Enallenols
Department of Organic Chemistry, Arrhenius Laboratory, Stockholm University, Stockholm, Sweden.
Department of Organic Chemistry, Arrhenius Laboratory, Stockholm University, Stockholm, Sweden.
Department of Materials and Environmental Chemistry, Arrhenius Laboratory, Stockholm University, Stockholm, Sweden.
Department of Materials and Environmental Chemistry, Arrhenius Laboratory, Stockholm University, Stockholm, Sweden.
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2020 (English)In: Organic Letters, ISSN 1523-7060, E-ISSN 1523-7052, Vol. 2, p. 417-421Article in journal (Refereed) Published
Abstract [en]

A palladium-catalyzed oxidative cascade carbonylative carbocyclization of enallenols was developed. Under mild reaction conditions, a range of cis-fused [5,5] bicyclic γ-lactones and γ-lactams with a 1,3-diene motif were obtained in good yields with high diastereoselectivity. The obtained lactone/lactam products are viable substrates for a stereoselective Diels-Alder reaction with N-phenylmaleimide, providing polycyclic compounds with increased molecular complexity.

Place, publisher, year, edition, pages
American Chemical Society (ACS), 2020. Vol. 2, p. 417-421
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Natural Sciences
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URN: urn:nbn:se:miun:diva-40677DOI: 10.1021/acs.orglett.9b04134Scopus ID: 2-s2.0-85078504450OAI: oai:DiVA.org:miun-40677DiVA, id: diva2:1507187
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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