Research shows highly enantioselective oxidation in olefins and organosulfur compounds using a chiral Mn(II) catalyst, suggesting its effectiveness for synthetic applications.
Described herein is the application of a chiral Mn(II) catalyst (6) derived from the commercially available chiral diamine trans-1,2-diaminocyclohexane to the highly enantioselective oxidation of a variety of mono-, di-, and trisubstituted olefins or various organosulfur(II) compounds.
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Reddy et al. (2026) studied this question.
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