Pyrolysis reactions of nonafluorobiphenyl-4-yl prop-2-enyl ether: A remarkable rearrangement reaction of an intramolecular Diels-Alder product
The pyrolysis reaction of nonafluorobiphenyl-4-yl prop-2-enyl ether were studied. The reaction was proposed as a remarkable rearrangement reaction of an intramolecular Diels-Alder product. The flash vapor pyrolysis of the compound performed at 350 °C gave a complex mixture containing the products obtained from Diels-Alder reactions. The molecular structure of the compounds obtained was characterized by x ray crystallography.
Batsanov, Andrei S.,Brooke, Gerald M.,Holling, Darren,Kenwright, Alan M.
Pyrolysis reactions of 4-nonafluorobiphenyl prop-2-enyl ether: A remarkable rearrangement reaction
The formation of the unexpected bicyclic compound 16 via the pyrolytic isomerisation of 4-nonafluorobiphenyl prop-2-enyl ether 8 can be rationalised by invoking the intermediacy of a rare retro-cyclisation reaction of the internal Diels-Alder adduct 12 (f
Batsanov, Andrei S.,Brooke, Gerald M.,Holling, Darren,Kenwright, Alan M.