924904-18-7

Upstream product

• 74-88-4 methyl iodide 
• 105259-27-6 2-(bromomethyl)-3-(methoxy)naphthalene 
• 13041-60-6 methyl 3-methoxy-2-naphthoate 
• 39110-92-4 (3-methoxy-naphthalen-2-yl)-methanol 
• 95033-74-2 (-)-10,10'-dihydroxy-9,9'-biphenanthryl 
• 80-48-8 methyl p-toluene sulfonate 
• 105259-38-9 2-(3-Methoxy-naphthalen-2-ylmethyl)-malonic acid 
• 105259-28-7 methyl 3-methoxy-2-naphthalenepropionate 
• 105259-39-0 3-(3-Methoxy-naphthalen-2-yl)-propionic acid 
• 105259-34-5 10-methoxy-1,2,3,4-tetrahydrophenanthrene 
• 105259-31-2 2-(3-cyanopropyl)-3-methoxynaphthalene 
• 105259-30-1 2-(3-bromopropyl)-3-methoxynaphthalene 
• 105259-29-8 3-methoxy-2-naphthalenepropanol 
• 105259-33-4 10-methoxy-1,2,3,4-tetrahydro-4-phenanthrenone 

Relevant academic research and scientific papers

Enantioselective oxidative-coupling of polycyclic phenols

Enantioselective oxidative-coupling of polycyclic phenols, such as 2-anthracenol, 9- or 3-phenanthrol, and 5-chrysenol was established by using vanadium(V/IV) catalysis under air or O2 as a co-oxidant. In the vanadium catalyzed reaction, the co