| Literature DB >> 31967396 |
Baoyu Xue1, Junhong Zhao1, Yange Fan1, Shipeng Chen1, Wenfeng Li1, Jin Chen1, Zheng Li1, Hongxing Wang1, Hongjun Kong1.
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.Entities:
Keywords: Docetaxel; Taxol; synthesis; taxane compounds
Mesh:
Substances:
Year: 2020 PMID: 31967396 DOI: 10.1002/cbdv.201900631
Source DB: PubMed Journal: Chem Biodivers ISSN: 1612-1872 Impact factor: 2.408