New Insights into Cyclobutenone Rearrangements: A Total Synthesis of the Natural ROS-Generating Anti-Cancer Agent Cribrostatin 6

Added on:
14 Nov, 2011

Aryl- and heteroarylcyclobutenone rearrangements proceed in excellent yield under continuous-flow conditions. The former shows a Hammett correlation with σI providing strong evidence that electrocyclisation is the rate-determining step and has a late transition state. The reaction has been modelled by using DFT and CCSD(T) methods, with the latter giving excellent correlation with the experimental rate constant. A short and efficient total synthesis of cribrostatin 6, an anti-neoplastic and anti-microbial agent, provides a topical demonstration of the value of this method.

  • Mubina Mohamed1
  • Théo P. Gonçalves1
  • Prof. Richard J. Whitby1
  • Dr. Helen F. Sneddon2
  • Prof. David C. Harrowven1
  • 1 Chemistry, University of Southampton, UK
  • 2 GlaxoSmithKline Medicines Research Centre, UK
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