前往化源商城

Studies on the reaction mechanism of the photocyclization of N-aryl enamines. Dependence of quantum yields on back and side reactions

T Wolff, R Waffenschmidt

文献索引:Wolff, Thomas; Waffenschmidt, Reinhard Journal of the American Chemical Society, 1980 , vol. 102, # 19 p. 6098 - 6102

全文:HTML全文

被引用次数: 14

摘要

Abstract: The photocyclization of 1-(N-methylanilino)-3, 4-dihydronaphthalene (l), 1-(N- methyiani1ino)-1-phenyl-1-propene (3), and 1-(N-methy1anilino)-1-phenyl-1-butene (4) in diethyl ether and methylcyclohexane (MCH) was investigated as a function of temperature. Decay kinetics of intermediates and relative quantum yields of product and intermediate formation were measured by using flash photolysis and steady irradiation experiments. In ...