107913-79-1

Upstream product

• 107913-78-0 2-<2-<2,4-bis<<2-(trimethylsilyl)ethoxy>methoxy>phenyl>-2-propenyl>-3,5-dimethoxy-4-(3-methyl-2-butenyl)phenol acetate 

Downstream Products

• 107913-86-0 3-[2,4-Bis-(tert-butyl-dimethyl-silanyloxy)-phenyl]-5,7-dimethoxy-6-(3-methyl-but-2-enyl)-chroman 
• 107913-87-1 6-<3,4-dihydro-5,7-dimethoxy-6-(3-methyl-2-butenyl)-2H-1-benzopyran-3-yl>-3-<<(1,1-dimethylethyl)dimethylsilyl>oxy>-2-(3-methyl-2-butenyl)phenol 
• 108074-33-5 (+/-)-5-O-methyllicoricidin 
• 107913-85-9 2-<3,4-dihydro-5,7-dimethoxy-6-(3-methyl-2-butenyl)-2H-1-benzopyran-3-yl>-5-<<(1,1-dimethylethyl)dimethylsilyl>oxy>phenol 
• 107913-84-8 Glyasperin D 
• 107913-82-6 <<4-<3,4-dihydro-5,7-dimethoxy-6-(3-methyl-2-butenyl)-2H-1-benzopyran-3-yl>-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