Heterogenisation of ketone catalysts within mesoporous supports for asymmetric epoxidation

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Abstract

The synthesis of the first mesoporous silica (150 Å) anchored carbohydrate-derived chiral ketone is described. This new heterogeneous catalyst has been shown to be effective in the asymmetric epoxidation of olefins by oxone. The heterogeneous ketone catalyst has comparable activity to that of its homogeneous counterpart and returned enantioselectivities up to 90% e.e. © 2013 The Royal Society of Chemistry.

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Brown, L. J., Brown, R. C. D., & Raja, R. (2013). Heterogenisation of ketone catalysts within mesoporous supports for asymmetric epoxidation. RSC Advances, 3(3), 843–850. https://doi.org/10.1039/c2ra21837b

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