Biomeditsinskaya Khimiya.
Russian Academy of Medical Sciences.
Том 63.
2017.
С. 296-305
Simple and efficient one-pot synthesis of 5-substituted isoxazoles and pyrazoles has been developed. The formation of the target isoxazoles and pyrazoles is initiated by 1,2-nucleophilic addition of generated in situ hydroxylamine or hydrazine to α-acetylenic γ-hydroxyaldehydes with further intramolecular cyclization of the adducts. The protocols are associated with readily available substrates, simple procedure, short reaction time, and moderate to high yields. © 2017 Taylor & Francis.