1H- and13C-NMR detection of mono- and dihydro-peroxide formation
Springer Online Journal Archives 1860-2000
Chemistry and Pharmacology
Abstract 1H- and13C-NMR investigations revealed that prolonged oxidation of unsubstituted cyclohexene and tetralin, containing symmetrical and weak allylic and benzylic CH bonds, results in the formation of both mono- and dihydroperoxo derivatives.
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