129207-82-5Relevant articles and documents
A Convenient Synthesis of 3-Aryl-4H-benzopyranoisoxazol-4-ones
Litinas, Konstantinos E.,Nicolaides, Demetrios N.,Varella, Evangelia A.
, p. 769 - 774 (2007/10/02)
Regioselective 1,3-dipolar cycloaddition of nitrile oxides 5a-c to ethyl o-hydroxycinnamate (3) gave the corresponding ethyl trans-3-aryl-4,5-dihydro-5-(2-hydroxyphenyl)-4-isoxazolecarboxylates 6a-c.Their structure was confirmed by reductive cleavage to 1 and compounds 9a-c.Compounds 6a-c afforded upon heating in the presence of pyridine the 3-aryl-4H-benzopyranoisoxazol-4-ones 11a-c.Compound 10c was also isolated from 6c and transformed thermally into 11c.