52528-97-9

Upstream product

• 39032-14-9 1-[(E)-2-(4-methoxyphenyl)ethenyl]-3-methoxybenzene 
• 59586-27-5 4-((3-methoxyphenyl)ethyl)phenol 
• 77-78-1 dimethyl sulfate 
• 72311-12-7 (3-methoxybenzyl)triphenylphosphonium bromide 
• 94534-13-1 (E)-4-methoxy-α-(3'-methoxyphenylmethylene)benzeneacetic acid 
• 591-31-1 3-methoxy-benzaldehyde 
• 39032-14-9 3,4'-Dimethoxystilben 
• 60815-18-1 diethyl [(3-methoxyphenyl)methyl]phosphonate 
• 105-13-5 4-Methoxybenzyl alcohol 
• 104-47-2 p-methoxybenzylnitrile 
• 10259-22-0 ethyl 3-methoxybenzoate 
• 52528-95-7 2-p-Methoxyphenyl-2-m-methoxybenzoylessigsaeureaethylester 
• 52528-94-6 3-(3-methoxyphenyl)-2-(4-methoxyphenyl)-3-oxopropanenitrile 
• 17274-18-9 sodium 2-(4-methoxyphenyl)acetate 

Downstream Products

• 37116-80-6 lunularin 
• 52528-89-9 3,4'-bis-benzoyloxy-bibenzyl 

Relevant academic research and scientific papers

Chromium-Salen Complex/Nitroxyl Radical Cooperative Catalysis: A Combination for Aerobic Intramolecular Dearomative Coupling of Phenols

We describe an aerobic intramolecular dearomative coupling reaction of tethered phenols using a catalytic system consisting of a chromium-salen (Cr-salen) complex combined with a nitroxyl radical. This novel catalytic system enables formation of various spirocyclic dienone products including those unable to be accessed by previously reported methods efficiently under mild reaction conditions.

Riccardin C derivatives as anti-MRSA agents: Structure-activity relationship of a series of hydroxylated bis(bibenzyl)s

Members of a series of macrocyclic bis(bibenzyl) riccardin-class derivatives were found to exhibit antibacterial activity towards methicillin-resistant Staphylococcus aureus (anti-MRSA activity). Structure-activity relationship (SAR) studies were conducted, focusing on the number and position of the hydroxyl groups. The minimum essential structure for anti-MRSA activity was also investigated.

TERPENOIDS AND BIBENZYLS FROM SOME NEW ZEALAND LIVERWORTS

Four liverworts, Marchantia berteroana, M. foliacea, Plagiochila stephensoniana and Porella elegantula collected in New Zealand were chemically investigated.M. berteroana contains cuparene and (-)-2-hydroxycuparene as the major components. γ-Cadinene is the major component of M. foliacea. 4-Hydroxy-3'-methoxybibenzyl is a chemical marker for P. stephensoniana which belongs to the non-pungent type of Plagiochila species.P. elegantula synthesizes perrottetianal and belongs to the non-pungent type of Porella species. - Key Word Index: Marchantia berteroana; M. foliacea; Plagiochila stephensoniana; Porella elegantula; Marchantiales; Jungermanniales; Hepaticae; terpenoids; 2-hydroxycuparene; perrottetianal; bibenzyls; 4-hydroxy-3'-methoxybibenzyl; chemosystematics.