16084-38-1

Upstream product

• 7249-36-7 2-(3,4-Dimethoxy-benzoyl)-4,5-dimethoxy-benzoic acid 
• 16462-68-3 iso-olivil dimethyl ether 
• 64-19-7 acetic acid 
• 4483-47-0 (+-)-1r-ethyl-3c-(3,4-dimethoxy-phenyl)-5,6-dimethoxy-2t-methyl-indan 
• 114574-46-8 (2-Dimethoxymethyl-4,5-dimethoxy-phenyl)-(3,4-dimethoxy-phenyl)-methanol 
• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 70461-33-5 2-bromo-4,5-dimethoxybenzaldehyde dimethyl acetal 

Downstream Products

• 7249-36-7 2-(3,4-Dimethoxy-benzoyl)-4,5-dimethoxy-benzoic acid 
• 117671-62-2 4,5-dimethoxy-2-veratryl-benzoic acid 
• 1025970-99-3 4-(3,4-Dimethoxy-phenyl)-9-hydroxy-6,7-dimethoxy-3H-naphtho[2,3-c]furan-1-one 

Relevant academic research and scientific papers

A simple method for the synthesis of 4-aryl-9-oxynaphthofuranone lignans

The 9-aryl-4-oxynaphthofuran-1(3H)-one system is generally synthesized in two steps from α-aryl-o-toluic acid derivatives. The method involves a tandem conjugate addition-Dieckmann type condensation between α-lithiated α-aryl-o-toluic acid derivatives and