Synthesis of 6-carbon termini-differentiated stereotriads via symchiral 2-trifloxy-1,3-cyclohexadiene monoepoxidel

DOI: 10.1016/S0040-4039(99)00343-3

Source and publish data:

Tetrahedron Letters p. 2699 - 2702 (1999)

Update date:2022-08-03

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Authors:

Hentemann, Murphy

Fuchs Fuchs

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Article abstract of DOI:10.1016/S0040-4039(99)00343-3

Jacobsen epoxidation of 2-trifloxy-1,3-cyclohexadiene provides a valuable asymmetric monoepoxide product that can be readily manipulated to efficiently provide highly-functionalized symchiral cyclic and acyclic synthons.

Full text of DOI:10.1016/S0040-4039(99)00343-3

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