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- W2011196557 abstract "A notably higher diastereoselectivity is observed in the dimethyldioxirane epoxidation of chiral allylic alcohols when less polar solvent mixtures are employed; this is interpreted in terms of a dipolar transition state with OH association through hydrogen bonding to the dioxirane, for which a preferential dihedral angle of >130° is estimated." @default.
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- W2011196557 title "Solvent effects in the dimethyldioxirane oxidation of allylic alcohols: evidence for hydrogen bonding in the dipolar transition state of oxygen transfer" @default.
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