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- W3096759770 endingPage "221" @default.
- W3096759770 startingPage "215" @default.
- W3096759770 abstract "Abstract A halogen bond donor based on a 2,2’‐bipyridine framework has been synthesized, and used to catalyze Friedel−Crafts reactions of furans. Electrophiles used successfully in these reactions included various enones, an aldehyde, and a carboxylic acid anhydride. The yields of the reactions were generally good using a moderate catalyst loading (0.025 or 0.1 equiv.) at a relatively low temperature (room temp. or 50 °C) in acetonitrile. The catalyst used was designed with a biaryl scaffold so that if it indeed proved to be an efficient halogen bond donor organocatalyst, an enantioenriched version of it could potentially serve as a stereoselective catalyst. magnified image" @default.
- W3096759770 created "2020-11-09" @default.
- W3096759770 creator A5020168684 @default.
- W3096759770 creator A5049339155 @default.
- W3096759770 date "2020-11-18" @default.
- W3096759770 modified "2023-10-12" @default.
- W3096759770 title "Halogen Bond‐Catalyzed Friedel−Crafts Reactions of Furans Using a 2,2’‐Bipyridine‐Based Catalyst" @default.
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- W3096759770 doi "https://doi.org/10.1002/adsc.202001019" @default.
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