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• W4231523780 abstract "Abstract A palladium(II)‐catalyzed γ‐C−H amination of cyclic alkyl amines to deliver highly substituted azetidines is reported. The use of a benziodoxole tosylate oxidant in combination with AgOAc was found to be crucial for controlling a selective reductive elimination pathway to the azetidines. The process is tolerant of a range of functional groups, including structural features derived from chiral α‐amino alcohols, and leads to the diastereoselective formation of enantiopure azetidines." @default.
• W4231523780 created "2022-05-12" @default.
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• W4231523780 date "2018-02-22" @default.
• W4231523780 modified "2023-10-09" @default.
• W4231523780 title "Selective Reductive Elimination at Alkyl Palladium(IV) by Dissociative Ligand Ionization: Catalytic C(sp³ )−H Amination to Azetidines" @default.
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• W4231523780 doi "https://doi.org/10.1002/ange.201800519" @default.
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