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- W2000443602 abstract "We have discovered that N-sulfonyl oxaziridines react with a broad range of olefins in the presence of iron salts to afford 1,3-oxazolidines. This process provides access to 1,2-aminoalcohols with the opposite sense of regioselectivity produced from the copper-catalyzed oxyamination previously reported by our laboratories. Thus, either regioisomeric form of 1,2-aminoalcohols can easily be obtained from the reaction of oxaziridines with olefins, and the sense of regioselectivity can be controlled by the appropriate choice of inexpensive, nontoxic, first-row transition-metal catalyst." @default.
- W2000443602 created "2016-06-24" @default.
- W2000443602 date "2010-06-22" @default.
- W2000443602 modified "2023-09-25" @default.
- W2000443602 title "Iron-Catalyzed Aminohydroxylation of Olefins" @default.
- W2000443602 doi "https://doi.org/10.1055/s-0029-1220040" @default.
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