Photolysis of 2, 6-di-tert-butyl-4-alkylphenols with polyhalomethanes
RHS Wang
Index: Wang,R.H.S. Journal of Organic Chemistry, 1972 , vol. 37, p. 2771 - 2774
Full Text: HTML
Citation Number: 6
Abstract
The photolysis of lb in either carbon tetrachloride or bromotrichloromethane gave the cyclohexadienones 8 and 9b as well as a tert-butyl halide. The same products were obtained whether 300-or 350-nm light was used, but the use of 350-nm light resulted in a much lower conversion of lb. Rloreover, 10 was produced either by irradiating lb in bromotrichloromethane containing 10% methanol or by stirring a mixture of 8 in methanol ...
Related Articles:
13 C NMR study of 7, 7-disubstituted quinone methides
[Lycka, Antonin; Snobl, Dobroslav; Koutek, Bohumir; Pavlickova, Libuse; Soucek, Milan Collection of Czechoslovak Chemical Communications, 1981 , vol. 46, # 9 p. 2083 - 2090]