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Iodine-catalyzed synthesis of benzoxazoles using catechols, ammonium acetate, and alkenes/alkynes/ketones via C-C and C-O bond cleavage.

Jasem AboonajmiFarhad PanahiMina Aali HosseiniMahdi AberiHashem Sharghi
Published in: RSC advances (2022)
An efficient metal-free synthesis strategy of benzoxazoles was developed via coupling catechols, ammonium acetate, and alkenes/alkynes/ketones. The developed methodology represents an operationally simple, one-pot and large-scale procedure for the preparation of benzoxazole derivatives using molecular iodine as the catalyst.
Keyphrases
  • room temperature
  • ionic liquid
  • dual energy
  • minimally invasive
  • highly efficient
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  • carbon dioxide
  • magnetic resonance
  • single molecule
  • electron transfer