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- W4375851919 abstract "Abstract Chiral pentacarboxycyclopentadienyl bromide reagents were synthesized to accomplish enantioselective bromination of silyl enol ethers to give corresponding α-bromoketone products in good yields and up to 77% ee. A catalytic version of this reaction was also demonstrated through the combination of Lewis acid activators and diethyl 2,2-dibromomalonate as stoichiometric achiral bromine source." @default.
- W4375851919 created "2023-05-10" @default.
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- W4375851919 date "2023-05-08" @default.
- W4375851919 modified "2023-10-17" @default.
- W4375851919 title "Enantioselective Bromination of Silyl Enol Ethers with Chiral Pentacarboxycyclopentadienyl Bromide" @default.
- W4375851919 cites W2151268707 @default.
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- W4375851919 doi "https://doi.org/10.1055/a-2088-9219" @default.
- W4375851919 hasPublicationYear "2023" @default.
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