116512-96-0

Upstream product

• 108-46-3 recorcinol 
• 151884-07-0 2',4'-dihydroxy-3-chloropropiophenone 
• 621-59-0 isovanillin 
• 76240-27-2 7-hydroxy-2,3-dihydro-4H-chromen-4-one 

Downstream Products

• 162290-04-2 (+/-)-7-hydroxy-3-(3'-hydroxy-4'-methoxybenzyl)chroman 
• 111254-38-7 (3aR,9bS)-7-Benzyloxy-3a-(3-benzyloxy-4-methoxy-benzyl)-2,2-dimethyl-3a,9b-dihydro-4H-[1,3]dioxolo[4,5-c]chromene 
• 111276-59-6 C₃₁H₂₆O₆ 
• 111254-39-8 (3aR,9bS)-3a-(3-Hydroxy-4-methoxy-benzyl)-2,2-dimethyl-3a,9b-dihydro-4H-[1,3]dioxolo[4,5-c]chromen-7-ol 
• 111254-35-4 (+/-)-7-benzyloxy-3,4-dihydroxy-3-(3'-benzyloxy-4-methoxybenzyl)-chroman 
• 111254-33-2 7-benzyloxy-3-(3'-benzyloxy-4'-methoxybenzylidene)-chroman-4-one 

Relevant academic research and scientific papers

Vanadium-Catalyzed Oxidative Intramolecular Coupling of Tethered Phenols: Formation of Phenol-Dienone Products

A mild and efficient method for the vanadium-catalyzed intramolecular coupling of tethered free phenols is described. The corresponding phenol-dienone products are prepared directly in good yields with low catalyst loadings. Electronically diverse tethered phenol precursors are well tolerated, and the catalytic method was effectively applied as the key step in syntheses of three natural products and a synthetically useful morphinan alkaloid precursor.

Isolation, synthesis, and bioactivity of homoisoflavonoids from Caesalpinia pulcherrima

One new homoisoflavonoid, (3E)-2,3-dihydro-6,7-dimethoxy-3[(3-hydroxy-4- methoxyphenyl)methylene]-4H-1-benzopyran-4-one and four naturally new analogues, (3E)-3-(1,3-benzodioxol-5-ylmethylene)-2,3-dihydro-7-hydroxy-4H-1-benzopyran-4- one, (3E)-3-(1,3-benz

NOVEL 3-BENZYLIDINE AND 3-BENZYL SUBSTITUTED CHROMANONES

The present invention provides novel chromanone derivatives that are useful for the treatment of inflammatory diseases, cancer and age-related macular degeneration