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- W2553608878 abstract "Dinosylated α-d-glucopyranoside was directly transformed into α-d-altropyranosides via in situ formed N-4-nosyl Hough-Richardson aziridine with nitrogen nucleophiles under mild conditions in fair to excellent yields. The scope of the aziridine ring-opening reaction was substantially broadened contrary to the conventional methods introducing solely the azide anion at high temperatures. If necessary, the N-4-nosyl Hough-Richardson aziridine can be isolated by filtration in a very good yield and high purity." @default.
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- W2553608878 date "2016-12-09" @default.
- W2553608878 modified "2023-09-26" @default.
- W2553608878 title "Ring-Opening Reactions of the <i>N</i>-4-Nosyl Hough–Richardson Aziridine with Nitrogen Nucleophiles" @default.
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- W2553608878 doi "https://doi.org/10.1021/acs.joc.6b01942" @default.
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