ARACHIDONATE EPOXXGENASE: TOTAL SYNTHESIS OF BOTH ENANTIOMERS OF 8,9- AND 11,12-EPOXYEICOSATRIENOIC ACID

DOI: 10.1016/S0040-4039(00)85391-5

Source and publish data:

Tetrahedron Letters p. 6035 - 6038 (1986)

Update date:2022-08-04

Topics:

Authors:

Mosset, Paul

Yadagiri, Pendri

Lumin, Sun

Capdevila, Jorge

Falck, J. R.

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Article abstract of DOI:10.1016/S0040-4039(00)85391-5

Both enantiomers of the epoxygenase metabolites 8,9- and 11,12-epoxyeicosatrienoic acid (EET) were synthesized by a convergent strategy utilizing dimethyl D- or L-malate and erythrospecific epoxidation.

Full text of DOI:10.1016/S0040-4039(00)85391-5

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