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- W1964669188 abstract "The authors describe the development of a palladium-catalyzed intermolecular cycloaddition that involves a nucleophliic ring closure to the central carbon of a π-allylpalladium intermediate. Spiro[2,4]heptanes are obtained in good yields and moderate diastereoselectivities using small phosphite ligands. If bulky phosphine ligands are used, a selective [4+2] cycloaddition occurs, leading to exo-methylene cyclohexane products." @default.
- W1964669188 created "2016-06-24" @default.
- W1964669188 date "2008-02-21" @default.
- W1964669188 modified "2023-10-18" @default.
- W1964669188 title "Catalytic Nucleophilic Ring Closure ofπ-Allylpalladium Intermediates" @default.
- W1964669188 doi "https://doi.org/10.1055/s-2008-1042691" @default.
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