Abstract
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.
Original language | English (US) |
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Pages (from-to) | 6035-6038 |
Number of pages | 4 |
Journal | Tetrahedron Letters |
Volume | 27 |
Issue number | 50 |
DOIs | |
State | Published - 1986 |
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry