749256-67-5Relevant articles and documents
Simple synthesis of sakuranetin and selinone via a common intermediate, utilizing complementary regioselectivity in the deacetylation of naringenin triacetate
Yamashita, Yasunobu,Hanaya, Kengo,Shoji, Mitsuru,Sugai, Takeshi
, p. 961 - 965 (2016)
Sakuranetin and selinone were successfully synthesized utilizing the regioselective deacetylation of naringenin triacetate. Deacetylation of the latter at C-7 with imidazole in 1,4-dioxane at 40°C furnished the corresponding diacetate in 80% yield. Methyl