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A Concise Total Synthesis of Deoxyschizandrin and Exploration of Its Antiproliferative Effects and those of Structurally Related Derivatives

  • Shaojun Zheng
  • , Sarah J. Aves
  • , Luca Laraia
  • , Warren R. J. D. Galloway
  • , Kurt G. Pike
  • , Wenjun Wu
  • , David R. Spring
  • University of Cambridge
  • AstraZeneca
  • Northwest Normal University

Research output: Contribution to journalJournal articleResearchpeer-review

Abstract

The natural product deoxyschizandrin has been shown to have a wide range of biological activities. In recent years the therapeutic potential of this compound against cancers has attracted significant interest. Herein we describe a concise de novo total synthesis of deoxyschizandrin based around a double organocuprate oxidation strategy. In addition, we present the results of biological studies exploring the ability of deoxyschizandrin and synthetic precursors lacking the medium ring biaryl unit to inhibit the proliferation of a human cancer cell line. These studies led to the identification of a structurally novel agent with in vitro anticancer activity.
Original languageEnglish
JournalChemistry - A European Journal
Volume18
Issue number11
Pages (from-to)3193-3198
ISSN0947-6539
DOIs
Publication statusPublished - 2012
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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