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- W2911689993 abstract "Olefin shuffle for just a nickel Controlling the geometry of carbon-carbon double bonds is a central component of chemical manufacturing. One useful trick is to shift hydrogen atoms around to interconvert C=C isomers selectively. However, this approach typically requires precious metals. Kapat et al. now report that more-abundant nickel can catalyze rapid conversion of terminal olefins into internal olefins with high selectivity for trans geometry. The odd-electron nickel complex relies on a radical mechanism to shuttle hydrogen to the terminal carbon from the saturated carbon adjacent to the double bond. Science , this issue p. 391" @default.
- W2911689993 created "2019-02-21" @default.
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- W2911689993 date "2019-01-25" @default.
- W2911689993 modified "2023-10-16" @default.
- W2911689993 title "<i>E</i> -Olefins through intramolecular radical relocation" @default.
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- W2911689993 doi "https://doi.org/10.1126/science.aav1610" @default.
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- W2911689993 hasPublicationYear "2019" @default.
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