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- W2172458996 abstract "Chiral aminoalkyl epoxyaziridine 1 is synthesized in high yield and diastereoselectivity from l-serine. Ring opening of epoxyaziridine 1 with primary amines is carried out with total chemo- and regioselectivity, affording chiral polyfunctionalized piperidines 8. The structure of these trisubstituted piperidines is established by NMR studies." @default.
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- W2172458996 date "2004-08-17" @default.
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- W2172458996 title "Synthesis of Chiral Amino Epoxyaziridines: Useful Intermediates for the Preparation of Chiral Trisubstituted Piperidines" @default.
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- W2172458996 doi "https://doi.org/10.1021/jo0490806" @default.
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