trans-2-Octene undergoes epoxidation with two manganese(III) porphyrin complexes by meta-chloroperbenzoic acid under catalytic reaction conditions in various solvents[1].
Chemistry (Weinheim an der Bergstrasse, Germany), 19(5), 1810-1818 (2012-11-28)
The participation of multiple active oxidants generated from the reactions of two manganese(III) porphyrin complexes containing electron-withdrawing and -donating substituents with peroxyphenylacetic acid (PPAA) as a mechanistic probe was studied by carrying out catalytic oxidations of cyclohexene, 1-octene, and ethylbenzene
The journal of physical chemistry. A, 119(28), 7559-7577 (2015-02-25)
The high pressure and temperature oxidation of methyl trans-2-nonenoate, methyl trans-3-nonenoate, 1-octene, and trans-2-octene are investigated experimentally to probe the influence of the double bond position on the chemical kinetics of long esters and alkenes. Single pulse shock tube experiments
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