132607-73-9Relevant academic research and scientific papers
Electrophilic substitutions by 2,2-bis(trifluoromethyl)ethylene-1,1-dicarbonitrile via addition
Brueckner, Reinhard,Huisgen, Rolf
, p. 1871 - 1874 (2007/10/02)
The interaction of the title compound (BTF) with unsaturated nucleophiles (ketene dithioacetals, α-substituted vinyl ethers, N-vinylcarboxamides, enols, furans, N-methylpyrrole, N-methylindole) effects substitution of vinylic or aromatic H by -C(CF3
2,2-BIS(TRIFLUOROMETHYL)ETHYLENE-1,1-DICARBONITRILE AND STYRENES. A DICHOTOMY OF CYCLOADDITION PATHWAYS
Brueckner, Reinhard,Huisgen, Rolf,Schmid, Joerg
, p. 7129 - 7132 (2007/10/02)
The title compounds undergo reversible Diels-Alder reactions and irreversible cycloadditions.The nonaromatic Diels-Alder adducts were isolated and subjected to cycloadditions with N-methyl-triazolinedione.
