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- W4251609796 abstract "Abstract An enantioselective catalytic alkoxylation/oxidative rearrangement of allylic alcohols has been established by using a Brønsted acid and chiral organoiodine. The presence of 20 mol % of an ( S )‐proline‐derived C 2 ‐symmetric chiral iodine led to enantioenriched α‐arylated β‐alkoxylated ketones in good yields and with high levels of enantioselectivity (84–94 % ee )." @default.
- W4251609796 created "2022-05-12" @default.
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- W4251609796 date "2019-04-29" @default.
- W4251609796 modified "2023-10-12" @default.
- W4251609796 title "Organoiodine‐Catalyzed Enantioselective Alkoxylation/Oxidative Rearrangement of Allylic Alcohols" @default.
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- W4251609796 doi "https://doi.org/10.1002/ange.201903007" @default.
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