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- W4301366320 endingPage "19237" @default.
- W4301366320 startingPage "19231" @default.
- W4301366320 abstract "The enantioselective synthesis of bis-homoallylic alcohols through nickel-catalyzed three-component fragment couplings of simple aldehydes, dienes, and aryl organoborons is disclosed. The reactions proceed through diene dicarbofunctionalization that concurrently forms two C-C bonds and two stereogenic centers. The transformations are promoted by a 5.0 mol % loading of a readily accessible chiral phosphine-nickel complex and afford products with high stereoselectivity." @default.
- W4301366320 created "2022-10-05" @default.
- W4301366320 creator A5057740779 @default.
- W4301366320 creator A5059776446 @default.
- W4301366320 date "2022-10-04" @default.
- W4301366320 modified "2023-10-11" @default.
- W4301366320 title "Efficient Enantio-, Diastereo, <i>E</i>/<i>Z</i>-, and Site-Selective Nickel-Catalyzed Fragment Couplings of Aldehydes, Dienes, and Organoborons" @default.
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- W4301366320 doi "https://doi.org/10.1021/jacs.2c08742" @default.
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- W4301366320 hasPublicationYear "2022" @default.
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