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- W2949747315 abstract "A directed, regiocontrolled hydroamination of unactivated terminal and internal alkenes is reported. The reaction is catalyzed by palladium(II) acetate and is compatible with a variety of nitrogen nucleophiles. A removable bidentate directing group is used to control the regiochemistry, prevent β-hydride elimination, and stabilize the nucleopalladated intermediate, facilitating a protodepalladation event. This method affords highly functionalized γ-amino acids in good yields with high regioselectivity." @default.
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- W2949747315 date "2016-09-01" @default.
- W2949747315 modified "2023-09-27" @default.
- W2949747315 title "ChemInform Abstract: Directed, Regiocontrolled Hydroamination of Unactivated Alkenes via Protodepalladation." @default.
- W2949747315 cites W2338622165 @default.
- W2949747315 doi "https://doi.org/10.1002/chin.201642042" @default.
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