Results in Chemistry (Jan 2024)

Design, stereoselective synthesis, and antitumoral activity of combretastatin A-4 analogs

  • Wilson P. da Silva,
  • Robrigo R.A. Caiana,
  • Maria E.S.B. Barros,
  • Juliano C.R. Freitas,
  • Paulo B.N. da Silva,
  • Gardenia G.C. Militão,
  • Roberta A. Oliveira,
  • Paulo H. Menezes

Journal volume & issue
Vol. 7
p. 101539

Abstract

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Combretastatin A-4 (CA-4) is a microtubule targeting agent, and it has a great advantage when compared to other compounds with a similar mechanism of action, such as vinca alkaloids, colchicine, podophillotoxin, and paclitaxel: its simpler structure. In this work, the stereoselective synthesis and antiproliferative activity of stable CA-4 analogs, obtained from the cross-coupling reaction between vinyl tellurides and potassium aryltrifluoroborates is described. The method is simple, fast, and general, allowing further applications for the synthesis of more complex compounds.

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