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Abstract
A new picture of the reaction mechanism of peracid epoxidation of olefins is proposed from the perspective of bond interaction. In contrast to the mechanism from the perspective of electronic theory, which includes the movement of an electron from the -bond to the negatively charged oxygen atom, the olefin is initially protonated and then migrates to the oxygen atom.
Supplementary materials
Title
Summarized results of the theoretical calculations
Description
Summarized results of the theoretical calculations
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