Journal of Labelled Compounds and Radiopharmaceuticals · 1989 · 13 citations · 8 references
Life SciencesBiochemistryChemistryNatural Product BiosynthesisOrganic ChemistrySteroid BiochemistryEicosanoid BiosynthesisLipid BiosynthesisOrganic SynthesisSteroid BiosynthesisArachidonic Acid BiosynthesisEicosanoid PrecursorsHydrogenationHydrogenation ReactionsProstaglandin AnaloguesProstaglandin E2 BiosynthesisProstaglandin F2alpha Biosynthesis
Abstract The complete chemical synthesis of unsaturated precursors of eicosanoids of series 1,2,3 is described. Selective hydrogenation by gaseous tritium of eicosapolyenoic acid acetylenic analogues was used to introduce the label into dihomo‐α‐linolenic, arachidonic and timnodonic acids, from which [ 3 H]PGE, [ 3 H]PGD and [ 3 H]TXB 2 were obtained by biosynthesis. From [ 3 H]PGE multiply labelled PGA, PGB, PGF α , PGI 2 ME, 6‐keto‐PGF 1α ME were synthesized by chemical methods.
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