128154-65-4

Upstream product

• 96-48-0 4-butanolide 
• 120-14-9 3,4-dimethoxy-benzaldehyde 

Downstream Products

• 97024-95-8 3-(3,4-Dimethoxybenzyl)-4,5-dihydro-2(3H)-furanone 
• 186411-98-3 2-[(3,4-dimethoxyphenyl)methylene]-1,4-butanediol 
• 169262-50-4 2-[(3,4-dimethoxyphenyl)methyl]butane-1,4-diol 
• 128154-72-3 3-(4,5-Dimethoxy-2-nitro-benzyl)-2,2-dimethyl-tetrahydro-furan 
• 128154-71-2 3-[1-(3,4-Dimethoxy-phenyl)-meth-(E)-ylidene]-2,2-dimethyl-tetrahydro-furan 
• 128154-68-7 3-(3,4-Dimethoxy-benzyl)-2,2-dimethyl-tetrahydro-furan 
• 1025839-71-7 Methanesulfonic acid 2-[1-(3,4-dimethoxy-phenyl)-meth-(E)-ylidene]-4-methanesulfonyloxy-butyl ester 

Relevant academic research and scientific papers

Facile stereoselective synthesis of (E)- and (Z)-α-substituted cinnamates: stereospecific dehydration reaction with 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC) and copper(II) chloride

A highly stereoselective method for the synthesis of (E)- and (Z)-α-substituted cinnamates in good yield has been achieved by?dehydration reaction of anti- and syn-α-substituted-β-hydroxyphenylpropiolate using EDC. This facile method has been used to synt

Facile Stereoselective Synthesis of (E)- and (Z)-α-Substituted Cinnamates by Stereoselective Dehydration Reaction with 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC)

Highly stereoselective syntheses of (E)- and (Z)-α-substituted cinnamates have been achieved by dehydration reaction of anti- and syn-α-substituted-β-hydroxyphenylpropionates with EDC in good yields. This facile method has been applied to the stereoselect

Evaluation of some benzyl and benzylidene monosubstituted γ-butyrolactones and tetrahydrofurans as platelet activating factor antagonist agents

Some benzyl and benzylidene monosubstituted γ-butyrolactones and tetrahydrofurans were applied as platelet activating factor (PAF) antagonist agents. The results indicated that, whereas all benzyl derivatives are completely inactive, benzylidene substitut