Palladium-Catalyzed Decarboxylative Asymmetric Allylic Alkylation of Thietane 1,1-Dioxides

Laidlaw, Gillian and Franckevicius, Vilius (2022) Palladium-Catalyzed Decarboxylative Asymmetric Allylic Alkylation of Thietane 1,1-Dioxides. Organic Letters, 24 (1). pp. 400-405. ISSN 1523-7060

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A palladium-catalyzed decarboxylative asymmetric allylic alkylation of thietane 1,1-dioxides via linear enolate intermediates from racemic starting materials has been developed. This process installs an α-sulfonyl tetrasubstituted stereogenic center with high enantioselectivity. The potential to transform the alkylated products to novel types of enantioenriched spirocycles for medicinal chemistry applications has also been demonstrated.

Item Type:
Journal Article
Journal or Publication Title:
Organic Letters
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This document is the Accepted Manuscript version of a Published Work that appeared in final form in Organic Letters, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see
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?? biochemistryorganic chemistryphysical and theoretical chemistry ??
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10 Jan 2022 11:50
Last Modified:
15 Jul 2024 22:13