Areneoxides and trans-dihydrodiols at the 5,6- and 7,8-positions of quinoline have been synthesized. High stability of both areneoxides allowed identification of the 5,6-oxide as a liver microsomal metabolite of quinoline. Both areneoxides are converted to trans-dihydrodiols by microsamal epoxide hydrolase.
Non-enzymatic hydration, amine addition, and oxidation reactions of aza-arene oxides
作者:Derek R. Boyd、R. Jeremy H. Davies、Robert Dunlop、H. Patricia Porter、Lynne Hamilton、John J. McCullough
DOI:10.1039/c39890000163
日期:——
The 5,6- and 7,8-arene oxides of quinoline were found to undergo unusual additionreactions with water and primary amines at ambient tempreature to yield trans-dihydrodiol and trans-hydroxyamine adducts respectively; oxygen atom addition yielded N-oxide and trans-5,6,7,8-dioxide derivatives.