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• W2021001835 abstract "The reactivity of the Z-protected aziridine derived from aspartic acid has been studied with various N- and O-nucleophiles. The optimized reaction conditions allow quick and easy access to 1, 2-diamines or amino alcohols. In the case of opening with N-nucleophiles, very good regioselectivity was observed. Use of an α-amino ester as the nucleophile yielded a methyleneamino pseudodipeptide." @default.
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• W2021001835 date "2006-04-01" @default.
• W2021001835 modified "2023-10-18" @default.
• W2021001835 title "Aziridines derived from amino acids as synthons in pseudopeptide synthesis" @default.
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• W2021001835 doi "https://doi.org/10.1016/j.tet.2006.02.003" @default.
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