Abstract
Nitrile oxides were formed from nitro ketones using silica gel-supported sodium hydrogen sulfate (NaHSO4/SiO2) or Amberlyst 15 as solid acid catalyst, and then the corresponding 3-acylisoxaszoles were obtained by reacting with alkynes via the 1,3-dipolar [3+2] cycloaddition. These heterogeneous catalysts are easily separable from the reaction mixture and reused. This synthetic method provides a facile, efficient, and reusable production of 3-acylisoxazoles.
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Itoh, K. I., Hayakawa, M., Abe, R., Takahashi, S., Hasegawa, K., & Aoyama, T. (2021). A Facile Approach to the Synthesis of 3-Acylisoxazole Derivatives with Reusable Solid Acid Catalysts. Synthesis (Germany), 53(24), 4636–4643. https://doi.org/10.1055/a-1581-0235
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