39953-45-2

Upstream product

• 73111-01-0 4',5,7-triacetoxyflavan-4-one 
• 517892-89-6 acetic acid 7-acetoxy-2-(4-benzyloxy-phenyl)-4-oxo-chroman-5-yl ester 
• 1070715-07-9 1-[2-hydroxy-4,6-bis(methoxymethoxy)phenyl]-3-[4-(benzyloxy)phenyl]prop-2-en-1-one 
• 345891-63-6 rac-2-[4-(benzyloxy)phenyl]-5,7-dihydroxychroman-4-one 
• 65490-09-7 2'-hydroxy-4',6'-bis(methoxymethoxy)acetophenone 
• 4397-53-9 p-benzyloxybenzaldehyde 
• 556-82-1 3-methyl-2-buten-1-ol 
• 517892-90-9 (±)-5,7-diacetoxy-4'-hydroxyflavan-4-one 

Downstream Products

• 28116-98-5 rac-5,7-dihydroxy-2-[4-(3-methylbut-2-enyloxy)phenyl]chroman-4-one 

Relevant academic research and scientific papers

Simple synthesis of sakuranetin and selinone via a common intermediate, utilizing complementary regioselectivity in the deacetylation of naringenin triacetate

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

A simple synthesis of selinone, an antifungal component of Monotes engleri

A new synthesis of racemic 5,7-dihydroxy-2-[4-(3-methyl-but-2-enyloxy)-phenyl]chroman-4-one (selinone) (rac-1a) isolated from Monotes engleri GILG was accomplished by two routes starting from MOM-protected phloracetophenone (2).