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- W2950671966 abstract "For the first time a mild and efficient procedure has been developed for the C-3 selective ring opening, under biomimetic conditions, of 2,3-aziridino alcohols and their derivatives with nucleophiles such as aromatic thiols and amines catalyzed by β-cyclodextrin in water at room temperature to afford the corresponding β-amino sulfides and diamines with high regioselectivity in impressive yields. The use of cyclodextrin precludes the use of either acid or base and the catalyst can be recovered and reused." @default.
- W2950671966 created "2019-06-27" @default.
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- W2950671966 date "2006-08-01" @default.
- W2950671966 modified "2023-09-27" @default.
- W2950671966 title "C-3 Selective Ring Opening of 2,3-Aziridino Alcohols and Their Derivatives with Nucleophiles in the Presence of β-Cyclodextrin in Water." @default.
- W2950671966 cites W2144916594 @default.
- W2950671966 doi "https://doi.org/10.1002/chin.200631041" @default.
- W2950671966 hasPublicationYear "2006" @default.
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