Erbium triflate is able to afford vic-diacetates in better yields, lower catalyst amounts and shorter times than most of the reported methods. Therefore, the present procedure represents a valuable, general and environmentally benign procedure to prepare these compounds. © ARKAT.
CITATION STYLE
Dalpozzo, R., De Nino, A., Nardi, M., Russo, B., & Procopio, A. (2006). 1,2-diacetates by epoxide ring opening promoted by erbium(III) triflate. Arkivoc, 2006(6), 67–73. https://doi.org/10.3998/ark.5550190.0007.607
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