β-Elemene derivatives produced from SeO2-mediated oxidation reaction

R Soc Open Sci. 2020 May 13;7(5):200038. doi: 10.1098/rsos.200038. eCollection 2020 May.

Abstract

Herein, we report the first access of β-elemene derivatives through the SeO2-mediated oxidation reaction. Several new compounds were isolated through such a one-step reaction, and their structures were elucidated using various 2D-NMR techniques. This method provides easy access to multiple oxidative β-elemene derivatives in one single step and represents the first modifications on cyclohexyl ring of β-elemene. It is expected to open up the opportunity for future derivatization on cyclohexyl ring of β-elemene. The new compounds obtained above showed better anti-proliferation activities than β-elemene itself on several cancer cell lines. Among them, compound 17 shows the best activity in antiproliferation assays of A549 and U-87MG cell lines.

Keywords: SeO2; anti-proliferation; cyclohexyl ring modifications; β-elemene.

Associated data

  • figshare/10.6084/m9.figshare.c.4968689
  • Dryad/10.5061/dryad.cnp5hqc1w