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Potential Bile Acid Metabolites. XXI. A New Synthesis of Allochenodeoxycholic and Allocholic Acids.
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1993
Year
Bioorganic ChemistrySecondary MetaboliteOrganic ChemistryNew SynthesisSimultaneous Oxidation-dehydrogenation ReactionDiversity Oriented SynthesisAllocholic AcidsNew MethodDerivativesBiochemistryDiversity-oriented SynthesisMetabolomicsPharmacologyNatural Product SynthesisEnantioselective SynthesisBiliary TractNatural SciencesMedicineSynthetic Chemistry
A new method for the preparation of allochenodeoxycholic and allocholic acids is described. The key steps in the synthesis are 1) simultaneous oxidation-dehydrogenation reaction of 3α-hydroxy 5β-bile acid formyl esters with iodoxybenzene catalyzed by benzeneseleninic anhydride, 2) reductive allomerization at C-5 of the 1, 4-dien-3-oxo hydroxy acids with lithium/liq. ammonia, and 3) subsequent reduction of the resulting 3-oxo 5α-compounds with K-Selectride.