Chemo- and enantioselective epoxidation of enynes

DOI: 10.1016/S0040-4039(98)00838-7

Source and publish data:

Tetrahedron Letters p. 4425 - 4428 (1998)

Update date:2022-08-17

Topics:

Authors:

Cao, Guo-An

Wang, Zhi-Xian

Tu, Yong

Shi, Yian

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Article abstract of DOI:10.1016/S0040-4039(98)00838-7

High chemo- and enantioselectivity have been obtained for asymmetric epoxidation of conjugated enynes using a fructose-derived chiral ketone as catalyst and Oxone as oxidant.

Full text of DOI:10.1016/S0040-4039(98)00838-7

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