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- W2951298561 abstract "Iridium trichloride catalyzes the ring opening of epoxides by aryl, heterocyclic, or aliphatic amines under mild conditions. The reactions proceed at room temperature to afford the corresponding β-amino alcohols in excellent yields. In general, the aminolysis of cyclopentene oxide is faster than that of cyclohexene oxide in the presence of iridium trichloride as a catalyst." @default.
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- W2951298561 date "2009-07-14" @default.
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- W2951298561 title "Aminolysis of Epoxides Using Iridium Trichloride as an Efficient Catalyst" @default.
- W2951298561 doi "https://doi.org/10.1055/s-0029-1216899" @default.
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