Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1315624 | Journal of Fluorine Chemistry | 2007 | 9 Pages |
Abstract
A novel synthetic method for the preparation of α-fluoro- and the still unknown α-trifluoromethylacrylonitriles is elaborated. The reaction of α-fluorovinylbromides and α-trifluoromethylvinylbromides with CuCN leads to the title compounds in good to high yields. While the α-fluoroacrylonitriles were isolated as mixture of Z/E-isomers, the α-trifluoromethylacrylonitriles were obtained as pure Z-isomers. The α-trifluoromethylacrylonitriles are shown to be excellent dienophiles for Diels–Alder reactions.
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Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Valentine G. Nenajdenko, Vasiliy M. Muzalevskiy, Aleksey V. Shastin, Elizabeth S. Balenkova, Günter Haufe,