Diastereoselective 14beta-hydroxylation of baccatin III derivatives

J Org Chem. 2003 Dec 12;68(25):9773-9. doi: 10.1021/jo0347112.

Abstract

14beta-Hydroxybaccatin III, a compound with limited availability by natural sources, is the starting material for the synthesis of the second-generation anticancer taxoid ortataxel. The 7-tert-butoxycarbonyl (1a) and 7-triethylsilyl (1b) derivatives of 14beta-hydroxybaccatin III 1,14-carbonate were synthesized from 10-deacetylbaccatin III (3). The crucial steps were (a) the C(14)beta hydroxylation of the corresponding 13-oxobaccatin III derivatives by oxaziridine-mediated electrophilic oxidation and (b) the reduction of the C(13) carbonyl group with sodium or alkylammonium borohydrides. This protocol provides a practical way for the semisynthesis of ortataxel from 10-deacetylbaccatin III, a compound readily available from various yews.

MeSH terms

  • Alkaloids / chemistry*
  • Antineoplastic Agents, Phytogenic / chemical synthesis
  • Docetaxel
  • Hydroxylation
  • Molecular Structure
  • Oxidation-Reduction
  • Paclitaxel / analogs & derivatives
  • Stereoisomerism
  • Taxoids / chemistry*

Substances

  • Alkaloids
  • Antineoplastic Agents, Phytogenic
  • Taxoids
  • Docetaxel
  • baccatin III
  • 10-deacetylbaccatine III
  • Paclitaxel