Chemistry & Biodiversity · 2020 · 18 citations · 5 references
PharmacyChemistryMedicinal ChemistryNatural Product BiosynthesisOrganic ChemistrySynthetic Medicinal ChemistryPhenylpropanoid BiosynthesisTerpenoid BiosynthesisColumn ChromatographyMedicinal Chemistry ApplicationsNatural Product SynthesisProduction CostsSemisynthesis Of Natural ProductsSilica Gel Treatment
Abstract A mixture of taxols was prepared from 10‐deacetyl‐7‐xylosyltaxanes by three‐step reactions: redox, acetylation, and deacetylation. The mixture was separated by column chromatography on silica gel to afford Taxol, Taxol B (Cephalomannine) and Taxol C. The mixture of Taxol B and Taxol C was converted to Docetaxel by Schwartz's reagent. The structures of Taxol and Docetaxel were characterized by HPLC, 1 H‐NMR, 13 C‐NMR and MS. This synthetic process has expanded the source of biomass for the chemical semi‐synthesis of Taxol and Docetaxel, reduced the production costs, and increased the biomass resource of taxanes.
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Taxol from Pestalotiopsis microspora, an endophytic fungus of Taxus wallachiana
Gary A. Strobel, Xianshu Yang, Joe Sears et al. · Microbiology · 1996 · 601 citations