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- W3039576896 endingPage "8556" @default.
- W3039576896 startingPage "8542" @default.
- W3039576896 abstract "1,2-Dicarbofunctionalization of alkenes has emerged as an efficient synthetic strategy for preparing substituted molecules by coupling readily available alkenes with electrophiles and/or nucleophiles. Nickel complexes serve as effective catalysts owing to their tendency to undergo facile oxidative addition and slow β-hydride elimination, and their capability to access both two-electron and radical pathways. Two-component alkene functionalization reactions have achieved high chemo-, regio-, and stereoselectivities by tethering one of the coupling partners to the alkene substrate. Three-component reactions, however, often incorporate directing groups to control the selectivity. Only a few examples of directing-group-free difunctionalizations of unactivated alkenes have been reported. Therefore, great opportunities exist for the development of three-component difunctionalization reactions with broad substrate scopes and tunable chemo-, regio-, and stereoselectivities." @default.
- W3039576896 created "2020-07-10" @default.
- W3039576896 creator A5032981628 @default.
- W3039576896 creator A5083385014 @default.
- W3039576896 date "2020-07-02" @default.
- W3039576896 modified "2023-10-16" @default.
- W3039576896 title "Nickel-Catalyzed Dicarbofunctionalization of Alkenes" @default.
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