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- W2156868757 abstract "A series of D2-symmetric chiral trans-dioxoruthenium(VI) porphyrins can effect enantioselective epoxidation of trans-β-methylstyrene in up to 70% ee, and 76% ee is attained for the oxidation of cinnamyl chloride; the facial selection for the trans-alkenes epoxidation is explained by a ‘head-on approach’ model." @default.
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- W2156868757 date "1999-01-01" @default.
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- W2156868757 title "Enantioselective epoxidation of trans-disubstituted alkenes by D2-symmetric chiral dioxoruthenium(VI) porphyrins" @default.
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- W2156868757 doi "https://doi.org/10.1039/a808776h" @default.
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