96894-16-5

Upstream product

• 469-28-3 (+)-1-hydroxy-6-epipinoresinol 4',4''-di-O-methyl ether 
• 96894-13-2 (+)-1-acetoxypinoresinol 
• 20583-78-2 3,4-dimethoxy-cinnamic acid ethyl ester 
• 144918-25-2 (4S,5R)-4-(3,4-Dimethoxy-benzyloxymethyl)-5-(3,4-dimethoxy-phenyl)-dihydro-furan-3-one 
• 81426-15-5 (+)-1-acetoxypinoresinol 4''-O-methyl ether 
• 144918-24-1 (2R,3S)-3-(3,4-Dimethoxy-benzyloxymethyl)-2-(3,4-dimethoxy-phenyl)-4-methylene-tetrahydro-furan 
• 144918-21-8 ethyl 2-bromo-3-(3,4-dimethoxyphenyl)-3-(prop-2-ynyloxy)propanoate 
• 144918-22-9 ethyl rac-(2R,3R)-2-(3,4-dimethoxyphenyl)-4-methylenetetrahydrofuran-3-carboxylate 
• 144918-23-0 2-(3,4-dimethoxyphenyl)-3-(hydroxymethyl)-4-methylenetetrahydrofuran 
• 20583-78-2 ethyl (E)-3,4-dimethoxycinnamate 
• 56-23-5 tetrachloromethane 
• 7664-93-9 sulfuric acid 
• 64-19-7 acetic acid 
• 7553-56-2 iodine 

Downstream Products

• 1212517-63-9 (3aS)-1c,4c-bis-(2-bromo-4,5-dimethoxy-phenyl)-(6ac)-dihydro-furo[3,4-c]furan-3ar-ol 
• 124281-59-0 Acetic acid (1R,2R,3R)-3-acetoxymethyl-1-(3,4-dimethoxy-phenyl)-2-hydroxy-6,7-dimethoxy-1,2,3,4-tetrahydro-naphthalen-2-ylmethyl ester 
• 124281-62-5 C₂₇H₃₄O₈ 
• 124281-60-3 C₂₅H₃₂O₇ 
• 124281-61-4 [(4aR,10R,10aR)-10-(3,4-Dimethoxy-phenyl)-7,8-dimethoxy-2,2-dimethyl-4,4a,5,10-tetrahydro-naphtho[2,3-d][1,3]dioxin-10a-yl]-methanol 
• 124281-57-8 (1R,2R,3R)-1-(3,4-Dimethoxy-phenyl)-2,3-bis-hydroxymethyl-6,7-dimethoxy-1,2,3,4-tetrahydro-naphthalen-2-ol 
• 124281-58-9 (2S,3R,4R)-4-(3,4-Dimethoxy-benzyl)-3-hydroxymethyl-2-(3-methoxy-phenyl)-tetrahydro-furan-3-ol 
• 80900-39-6 2,5-bis(3,4-dimethoxyphenyl)-4-pyrone-3-aldehyde 
• 80900-41-0 2,5-bis(3,4-dimethoxyphenyl)-4-pyrone-3-carbinol 
• 252726-89-9 (1R,8S,9R,12S)-8-(3,4-Dimethoxy-phenyl)-12-hydroxymethyl-4,5-dimethoxy-11-oxa-tricyclo[7.2.1.0^2,7]dodeca-2,4,6-trien-12-ol 

Relevant academic research and scientific papers

Stereoselective Total Synthesis of (+/-)-Paulownin and (+/-)-Isogmelinol through Radical Annulation Route

A highly stereocontrolled synthesis of furofuran lignans, (+/-)-Paulownin (1a) and (+/-)-Isogmelinol (1b) is described involving intramolecular radical cyclisation as a key step.

Stereoselective Radical Annulation Route to the Synthesis of (+/-)-Paulownin und (+/-)-Isogmelinol

A highly stereocontrolled synthesis of (+/-)-Paulownin (1a) and (+/-)-isogmelinol (1b) is reported involving intramolecular radical cyclisation reaction as a key step.