123931-38-4Relevant articles and documents
A short catalytic enantioselective synthesis of the vascular antiinflammatory eicosanoid (11R,12S)-oxidoarachidonic acid
Han, Xiaojun,Crane, Sheldon N.,Corey
, p. 3437 - 3438 (2000)
(Equation presented) An effective pathway is described for the synthesis of (11R,12S)-oxidoarachidonic acid (1) from the achiral precursors shown.
ARACHIDONATE EPOXXGENASE: TOTAL SYNTHESIS OF BOTH ENANTIOMERS OF 8,9- AND 11,12-EPOXYEICOSATRIENOIC ACID
Mosset, Paul,Yadagiri, Pendri,Lumin, Sun,Capdevila, Jorge,Falck, J. R.
, p. 6035 - 6038 (2007/10/02)
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.