128375-97-3Relevant articles and documents
A new synthetic path to peri-naphthisoxazoles by oxidative intramolecular cyclization of some β,γ-unsaturated oximes
Barnes, John C.,Horspool, William M.,Hynd, George
, p. 425 - 426 (1999)
Some β,γ-unsaturated oximes undergo an unprecedented intramolecular cycloaddition to an aryl group to afford peri-naphthisoxazoles when they are irradiated in the presence of PhI(OAc)2 and I2 or HgO and I2 in benzene or by
Intramolecular Electron Transfer in the Novel Photoreaction of some β,γ-Unsaturated Oxime-Boron Trifluoride Complexes. A New Synthetic Path to Dihydroisoxazoles
Armesto, Diego,Barnes, John C.,Horspool, William M.,Langa, Fernando
, p. 123 - 125 (2007/10/02)
β,γ-Unsaturated oximes are photochemically reactive in benzene solution when irradiated in the presence of boron trifluoride-diethyl ether; typically 2,2-dimethyl-4,4-diphenylbut-3-enal oxime affords a low yield of 2,2-diphenyl-3,3-dimethylcyclopropanecar