94935-92-9

Upstream product

• 107913-73-5 3,5-dimethoxy-4-(3-methyl-2-butenyl)phenol tert-butyldimethylsilyl ether 
• 80902-65-4 2-(3-methylbuta-2-enyl)-1,3,5-trihydroxybenzene 
• 77-78-1 dimethyl sulfate 
• 500-99-2 3,5-dimethoxyphenol 
• 96700-91-3 3,5-dimethoxyphenol tert-butyldimethylsilyl ether 
• 870-63-3 prenyl bromide 

Downstream Products

• 107913-77-9 <<4-<1-<<3,5-dimethoxy-4-(3-methyl-2-butenyl)phenoxy>methyl>ethenyl>-1,3-phenylene>bis<<(oxymethylene)oxy>-2,1-ethanediyl>>bis(trimethylsilane) 

Relevant academic research and scientific papers

Total Synthesis of (+/-)-5-O-Methyllicoricidin

A novel intramolecular Mitsunobu alkylation is employed to construct the benzopyran moiety of the newly isolated isoflavan 5-O-methyllicoricidin.This convergent 15-step total synthesis outlines a chemically mild approach to the acid-sensitive isoflavanoid

STRUCTURES OF MULBERROFURANS B AND L, 2-ARYLBENZOFURAN DERIVATIVES FROM THE ROOT BARK OF THE CULTIVATED MULBERRY TREE (MORUS LHOU (SER.) KOIDZ.)

Mulberrofuran L, a new 2-arylbenzofuran derivative, was isolated from benzene extract of the cultivated mulberry tree (Japanese name "Roso", a cultivated variety of Morus lhou (SER.) KOIDZ), and the structure was shown to be 3 on the basis of the spectral and chemical data.The structure of mulberrofuran B was reversed from the structure (2) to 2' on the basis of the formation of 3 from 2'.