Total Synthesis of Paclitaxel

Org Lett. 2022 Jan 14;24(1):202-206. doi: 10.1021/acs.orglett.1c03851. Epub 2021 Dec 14.

Abstract

The total synthesis of paclitaxel (Taxol) is described. Double Rubottom oxidation of the bis(silyl enol ether) derived from a tricarbocyclic diketone effectively installed a bridgehead olefin and C-5/C-13 hydroxy groups in a one-step operation. The novel Ag-promoted oxetane formation smoothly constructed the tetracyclic framework of paclitaxel.

MeSH terms

  • Antineoplastic Agents, Phytogenic / chemical synthesis
  • Antineoplastic Agents, Phytogenic / chemistry
  • Antineoplastic Agents, Phytogenic / pharmacology
  • Molecular Structure
  • Oxidation-Reduction
  • Paclitaxel* / chemical synthesis
  • Paclitaxel* / chemistry
  • Stereoisomerism

Substances

  • Paclitaxel
  • Antineoplastic Agents, Phytogenic