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- W4244932781 endingPage "1713" @default.
- W4244932781 startingPage "1708" @default.
- W4244932781 abstract "Abstract A B(C 6 F 5 ) 3 ‐catalyzed hydroarylation of a series of 1,3‐dienes with various phenols has been established through a combination of theoretical and experimental investigations, affording structurally diverse ortho ‐allyl phenols. DFT calculations show that the reaction proceeds through a borane‐promoted protonation/Friedel–Crafts pathway involving a π‐complex of a carbocation–anion contact ion pair. This protocol features simple and mild reaction conditions, broad functional‐group tolerance, and low catalyst loading. The obtained ortho ‐allyl phenols could be further converted into flavan derivatives using B(C 6 F 5 ) 3 with good cis diastereoselectivity. Furthermore, this transformation was applied in the late‐stage modification of pharmaceutical compounds." @default.
- W4244932781 created "2022-05-12" @default.
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- W4244932781 date "2019-01-11" @default.
- W4244932781 modified "2023-10-15" @default.
- W4244932781 title "Chemoselective Borane‐Catalyzed Hydroarylation of 1,3‐Dienes with Phenols" @default.
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- W4244932781 doi "https://doi.org/10.1002/ange.201811729" @default.
- W4244932781 hasPublicationYear "2019" @default.
- W4244932781 type Work @default.