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- W4385655164 abstract "An efficient method for the enantioselective synthesis of 2,3-dihydrofurans bearing a quaternary stereocenter has been developed via Pd-catalyzed asymmetric allylic cycloaddition and a retro-Dieckmann Fragmentation cascade. The asymmetric allylic cycloaddition of vinylethylene carbonates with 3-cyanochromone followed by base-assisted retro-Dieckmann fragmentation proceeded smoothly via a one-pot process to produce chiral 3,4-disubstituted 2,3-dihydrofurans in high yields with excellent enantioselectivities." @default.
- W4385655164 created "2023-08-09" @default.
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- W4385655164 date "2023-08-08" @default.
- W4385655164 modified "2023-09-30" @default.
- W4385655164 title "Synthesis of Chiral 2,3-Dihydrofurans via One-Pot Pd-Catalyzed Asymmetric Allylic Cycloaddition and a Retro-Dieckmann Fragmentation Cascade" @default.
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- W4385655164 doi "https://doi.org/10.1021/acs.joc.3c00976" @default.
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