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- W4231763124 abstract "The enantioselective oxyarylation of (E)-6-aryl-1-silyloxylhex-3-ene was achieved using a lactate-based chiral hypervalent iodine(III) reagent in the presence of boron trifluoride diethyl etherate. The silyl ether promotes the oxidative cyclization, and enhances the enantioselectivity. In addition, the corresponding aminoarylation was achieved." @default.
- W4231763124 created "2022-05-12" @default.
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- W4231763124 date "2016-11-23" @default.
- W4231763124 modified "2023-10-16" @default.
- W4231763124 title "Metal-Free Enantioselective Oxidative Arylation of Alkenes: Hypervalent-Iodine-Promoted Oxidative C−C Bond Formation" @default.
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- W4231763124 doi "https://doi.org/10.1002/ange.201609110" @default.
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