939017-93-3

Upstream product

• 1746-89-0 2-allyl-1,3-dihydroxybenzene 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 57234-29-4 1,3-bis(methoxymethyl)resorcinol 
• 939017-92-2 2-allyl-1,3-bis(methoxymethoxy)benzene 

Downstream Products

• 939017-94-4 2-(2,6-bis(tert-butyldimethylsilyloxy)phenyl)acetaldehyde 
• 939017-95-5 ethyl (E)-4-(2,6-bis(tert-butyldimethylsilyloxy)phenyl)-2-methylbut-2-enoate 
• 939017-96-6 (E)-4-(2,6-bis(tert-butyldimethylsilyloxy)phenyl)-2-methylbut-2-en-1-ol 
• 939017-97-7 (E)-4-(2,6-bis(tert-butyldimethylsilyloxy)phenyl)-2-methylbut-2-enyl methyl carbonate 
• 939017-98-8 (E)-4-(2,6-dihydroxyphenyl)-2-methylbut-2-enyl methyl carbonate 

Relevant academic research and scientific papers

Stereoselective syntheses of the 2-isopropenyl-2,3-dihydrobenzofuran nucleus: Potential chiral building blocks for the syntheses of tremetone, hydroxytremetone, and rotenone

(Chemical Equation Presented) The first enantioselective synthesis of the 2-isopropenyl-2,3-dihydrobenzofuran skeleton of tremetone and hydroxytremetone from (E)-4-(2-hydroxyphenyl)-2-methyl-2-butenyl methyl carbonate and (E)-4-(2,6-dihydroxyphenyl)-2-met