80610-03-3Relevant academic research and scientific papers
Synthesis of 4H-chromene-isoxazole hybrids via ortho-hydroxy directing cyclization of isoxazole-styrenes and Michael addition of imino-chromenes in aqueous medium
Nagaraju, Sakkani,Sathish, Kota,Kashinath, Dhurke
supporting information, p. 1252 - 1258 (2021/03/06)
A green, efficient, and one-pot method synthesis of functionalized 4H-chromene-isoxazole hybrids is reported via o-hydroxy group directing cyclization of isoxazole-styrenes and Michael addition of 3,5-dimethyl-4-nitroisoxazole on 2-imino-2H-chromene-3-carbonitrile (independent methods). The developed methodology was further extended for nitromethane, malononitrile, and alkylcyanoacetates as Michael donors.
Fused Heterocycles. IV. Synthesis of 7-(o-Hydroxyphenyl)-3,5-dimethyl-7,8-dihydro-6H-isoxazoloazepines
Malla Reddi, Kooturu,Janakirama Rao, Citineni,Krishna Murthy, Ananthula
, p. 3617 - 3618 (2007/10/02)
Michael addition of acetylacetone to 3-methyl-4-nitro-5-(o-hydroxystyryl)isoxazoles gives 4-(o-acetoxyphenyl)-5-(3-methyl-4-nitro-5-isoxazoyl)-2-pentanones (4).Reductive cyclization of 4 with tin(II) chloride and concentrated hydrochloric acid leads to 7-
