Elsevier

Tetrahedron Letters

Volume 39, Issue 43, 22 October 1998, Pages 7819-7822
Tetrahedron Letters

Highly enantioselective epoxidation of enol silyl ethers and esters

https://doi.org/10.1016/S0040-4039(98)01711-0Get rights and content

Abstract

High enantioselectivities have been obtained for asymmetric epoxidation of enol silyl ethers and asters using a fructose-derived chiral ketone as catalyst and Oxone as oxidant.

High enantioselectivities have been obtained for asymmetric epoxidation of enol silyl ethers and esters using fructose-derived chiral ketone 1 as catalyst and Oxone as oxidant.

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