Molecules (Mar 2010)

Novel Oxidative Ring Opening Reaction of 1H-Isotelluro-chromenes to Bis(o-formylstyryl) Ditellurides

  • Mamoru Kaname,
  • Hirohito Satoh,
  • Kazuo Ohyanagi,
  • Haruki Sashida

DOI
https://doi.org/10.3390/molecules15031466
Journal volume & issue
Vol. 15, no. 3
pp. 1466 – 1472

Abstract

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The oxidation of 1-unsubstituted or 1-phenyl-1H-isotellurochromenes with m-chloroperbenzoic acid (mCPBA) in CHCl3 resulted in a ring opening reaction to produce as the sole products the corresponding o-formyl or benzoyl distyryl ditellurides, which were also produced by the hydrolysis of the 2-benzotelluropyrylium salts readily prepared from the parent isotellurochromene.

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