Abstract
Efficient reduction of mono- and disubstituted norbornyl α-diketones with zinc in [bmimBF4]:[H2O] to afford the corresponding acyloins in excellent yields and diastereoselectivities is described. In case of the monosubstituted norbornyl α-diketones, very high regioselectivities ranging from 90:10 to 100:0, in favor of diastereomer possessing endohydroxyl diagonal to endo-substituent were observed.
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APA
Khan, F. A., & Sudheer, C. (2009). An Efficient method for zinc mediated reduction of norbornyl α diketones in [bmim][BF4]:H2O. Arkivoc, 2009(7), 222–228. https://doi.org/10.3998/ark.5550190.0010.721
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