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- W2016266963 abstract "Allyl cyanides are found to add across alkynes in the presence of a nickel catalyst prepared from Ni(cod)2 and P(4-CF3−C6H4)3 in situ to give variously functionalized di- or trisubstituted acrylonitriles in highly stereoselective manners possibly via a π-allylnickel species as an intermediate. α-Siloxyallyl cyanides also react at the γ-position of a cyano group with both internal and terminal alkynes having various functional groups to give silyl enol ethers, which give the corresponding aldehydes or ketones upon hydrolysis." @default.
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- W2016266963 date "2006-10-10" @default.
- W2016266963 modified "2023-10-14" @default.
- W2016266963 title "Allylcyanation of Alkynes: Regio- and Stereoselective Access to Functionalized Di- or Trisubstituted Acrylonitriles." @default.
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- W2016266963 doi "https://doi.org/10.1002/chin.200641057" @default.
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