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- W2765262940 abstract "Enantiomerically pure, chiral secondary and tertiary aziridine alcohols (including the aziridine analogue of ProPhenol—AziPhenol) have proven to be highly effective catalysts for enantioselective asymmetric reactions in the presence of zinc ions, including arylation of aromatic aldehydes, epoxidation of chalcone and addition of diethylzinc to aldehydes, leading to the desired chiral products in high chemical yields (up to 90%) and with ee’s up to 90%. A higher catalytic activity of Prophenol-type bis(aziridine alcohol) in the aforementioned asymmetric transformations has been demonstrated." @default.
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- W2765262940 date "2017-12-01" @default.
- W2765262940 modified "2023-10-02" @default.
- W2765262940 title "Highly enantioselective asymmetric reactions involving zinc ions promoted by chiral aziridine alcohols" @default.
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- W2765262940 doi "https://doi.org/10.1016/j.tetasy.2017.10.007" @default.
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