476003-41-5

Upstream product

• 476003-35-7 methyl (E)-4-[2-(tert-butyldimethylsilyloxy)-5-(methoxymethoxy)phenyl]-2-methyl-2-butenoate 
• 476003-37-9 (2S,3S)-4-[2-(tert-butyldimethylsilyloxy)-5-(methoxymethoxy)phenyl]-2-methyl-2,3-epoxy-butan-1-ol 
• 476003-36-8 (E)-4-[2-(tert-butyldimethylsilyloxy)-5-(methoxymethoxy)phenyl]-2-methyl-2-buten-1-ol 
• 476003-54-0 3-[2-(tert-butyldimethylsilyloxy)-5-(methoxymethoxy)phenyl]propane-1,2-diol 
• 476003-34-6 1-(tert-butyldimethylsilyloxy)-2-(2-propenyl)-4-(methoxymethoxy)benzene 
• 476003-33-5 2-(2-propenyl)-4-(methoxymethoxy)phenol 
• 476003-32-4 allyl 4-(methoxymethoxy)phenyl ether 
• 123-31-9 hydroquinone 
• 57433-93-9 hydroquinone monomethoxymethyl ether 
• 21204-67-1 methyl (triphenylphosphoranylidene)acetate 

Downstream Products

• 476003-50-6 acetic acid 2-benzenesulfonyl-1-[2-(6-methoxymethoxy-2-methyl-2H-chromen-2-yl)-ethyl]-2,6-dimethyl-hept-5-enyl ester 
• 476003-49-3 4-benzenesulfonyl-1-(6-methoxymethoxy-2-methyl-2H-chromen-2-yl)-4,8-dimethyl-non-7-en-3-ol 
• 476003-42-6 (E)-3-[(2S,3S)-3-(2-Hydroxy-5-methoxymethoxy-benzyl)-2-methyl-oxiranyl]-acrylic acid methyl ester 

Relevant academic research and scientific papers

Total synthesis of both enantiomers of dictyochromenol and their (Z)-isomers.

Total syntheses of both enantiomers of dictyochromenol (1) and its (Z)-stereoisomer (2) were achieved with high enantiomeric purity. The results of this study reveal the relationship between the optical rotation of the resolved 1 enantiomers.