352019-93-3

Upstream product

• 100-39-0 benzyl bromide 
• 352019-92-2 2-allyl-4-bromo-6-methoxyphenol 
• 90-05-1 2-methoxy-phenol 

Downstream Products

• 352019-96-6 (4S)-4-benzyl-3-[(2S,3S)-2-(2-benzyloxy-5-bromo-3-methoxyphenyl)-3-(4-benzyloxy-3-methoxyphenyl)-3-hydroxypropionyl]-2-oxazolidinone 
• 352020-01-0 (2S,3R)-2-(4-tert-butyldimethylsilyloxy-3-methoxyphenyl)-3-tert-butyldimethylsilyloxymethyl-2,3-dihydro-5E-(3-ethoxy-3-oxo-1-propenyl)-7-methoxybenzo[b]furan 
• 352019-97-7 (1S,2R)-2-(2-benzyloxy-5-bromo-3-methoxyphenyl)-1-(4-benzyloxy-3-methoxyphenyl)-1,3-propanediol 
• 352020-00-9 (2S,3R)-2-(4-tert-butyldimethylsilyloxy-3-methoxyphenyl)-3-tert-butyldimethylsilyloxymethyl-2,3-dihydro-5-formyl-7-methoxybenzo[b]furan 
• 352019-99-9 (2S,3R)-5-bromo-2-(4-tert-butyldimethylsilyloxy-3-methoxyphenyl)-3-tert-butyldimethylsilyloxymethyl-2,3-dihydro-7-methoxybenzo[b]furan 
• 352020-02-1 (2S,3R)-5-[(E)-2-ethoxycarbonylvinyl]-2,3-dihydro-2-(4-hydroxy-3-methoxyphenyl)-3-hydroxymethyl-7-methoxybenzo[b]furan 
• 352019-95-5 (4S)-4-benzyl-3-[2-(2-benzyloxy-5-bromo-3-methoxyphenyl)acetyl]-2-oxazolidinone 
• 352019-98-8 (2S,3R)-5-bromo-2,3-dihydro-2-(4-hydroxy-3-methoxyphenyl)-3-hydroxymethyl-7-methoxybenzo[b]furan 
• 352019-94-4 (2-benzyloxy-5-bromo-3-methoxyphenyl)acetic acid 
• 97465-82-2 (2S,3R)-2,3-dihydro-2-(4-hydroxy-3-methoxyphenyl)-5-[(E)-3-hydroxy-1-propenyl]-3-hydroxymethyl-7-methoxybenzo[b]furan 

Relevant academic research and scientific papers

Stereoselective synthesis of the neolignan, (+ )-dehydrodiconiferyl alcohol.

A stereo controlled synthesis of the biologically active neolignan, (+)-dehydrodiconiferyl alcohol (1) was achieved. This synthetic method was also efficient for preparing its enantiomer and other derivatives with biological activity.