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Stereocontrolled Preparation of the C1-C14 Polyene Fragment of Benzenic Ansamycin Antibiotics Ansatrienin A and B
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1999
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Combinatorial ChemistryEngineeringOrganic ChemistryChemistryHeterocycle ChemistryPharmaceutical ChemistryMedicinal ChemistryOther Ansamycin AntibioticsStereoselective SynthesisC1-c14 Polyene FragmentBiochemistryPharmacologyNatural Product SynthesisBiomolecular EngineeringConsecutive Evans-aldol ReactionsNatural SciencesStereocontrolled PreparationCarbon BackboneSynthetic Chemistry
A practical synthesis of the C1-C14 polyene unit 5 in ansatrienin A (mycotrien I), 1a, and other ansamycin antibiotics is described which involves elaboration of the chiral unsaturated aldehyde 6 and phosphonate 7, followed by coupling of the building blocks by Horner-Emmons-olefination and Duthaler's aldolation. The synthesis of 6 successfully applies two consecutive Evans-aldol reactions for constructing the carbon backbone.