Highly Diastereoselective Palladium-Catalyzed Oxidative Cascade Carbonylative Carbocyclization of EnallenolsShow others and affiliations
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
National Category
Natural Sciences
Identifiers
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
2020-12-072020-12-072021-05-04Bibliographically approved