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- W4243632593 endingPage "4841" @default.
- W4243632593 startingPage "4837" @default.
- W4243632593 abstract "Abstract The first visible‐light‐promoted dearomative fluoroalkylation of β‐naphthols was realized without the assistance of any transition‐metal catalysts or external photosensitizers. Inexpensive fluoroalkyl iodides were directly used as efficient fluoroalkylation reagents under very mild reaction conditions. The scope of this process was found to be general and broad, and both trifluoromethyl and perfluoroalkyl groups (‐C 4 F 9 , ‐C 6 F 13 , and ‐C 8 F 17 ) were installed in excellent yields. Preliminary mechanistic studies suggest that visible‐light‐promoted intermolecular charge transfer within the naphtholate–fluoroalkyl iodide electron donor–acceptor (EDA) complex induces a single electron transfer in the absence of photocatalysts." @default.
- W4243632593 created "2022-05-12" @default.
- W4243632593 creator A5009240802 @default.
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- W4243632593 creator A5071811306 @default.
- W4243632593 creator A5078277278 @default.
- W4243632593 creator A5078998268 @default.
- W4243632593 date "2018-03-27" @default.
- W4243632593 modified "2023-10-14" @default.
- W4243632593 title "Visible‐Light‐Promoted Dearomative Fluoroalkylation of β‐Naphthols through Intermolecular Charge Transfer" @default.
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