110315-50-9

Upstream product

• 110-87-2 3,4-dihydro-2H-pyran 
• 110330-19-3 1-<(4,5-trans)-4,5-Dihydroxy-4-methyl-1-cyclohexen-1-yl>ethanon 
• 100938-99-6 1-(1-Methyl-7-oxabicyclo<4.1.0>hept-3-en-4-yl)ethanon 

Downstream Products

• 110315-51-0 1-<(4,5-trans)-4-Hydroxy-4-methyl-5-(tetrahydro-2-pyranyloxy)-1-cyclohexen-1-yl>ethanon 
• 94294-75-4 <1,2-trans,4(E)>-4-(1',5'-Dimethyl-4'-hexen-1'-yliden)-1-methyl-1,2-cyclohexandiol 
• 94294-76-5 <1,2-trans,4(Z)>-4-(1',5'-Dimethyl-4'-hexen-1'-yliden)-1-methyl-1,2-cyclohexandiol 
• 110315-47-4 (1,2-trans)-4-<1',5'-Dimethyl-1'-(tetrahydro-2''-pyranyloxy)-4'-hexen-1'-yl>-1-methyl-2-(tetrahydro-2'''-pyranyloxy)-4-cyclohexen-1-ol 
• 110315-45-2 (1,2-trans)-4-(1'-Hydroxy-1',5'-dimethyl-4'-hexen-1'-yl)-1-methyl-2-(tetrahydro-2''-pyranyloxy)-4-cyclohexen-1-ol 
• 110315-52-1 <1,2-trans,4(EZ)>-4-(1',5'-Dimethyl-4'-hexen-1'-yliden)-1-methyl-2-(tetrahydro-2''-pyranyloxy)-1-cyclohexanol 
• 110315-48-5 (1,2-trans)-4-(1',5'-Dimethyl-4'-hexen-1'-yl)-1-methyl-2-(tetrahydro-2''-pyranyloxy)-4-cyclohexen-1-ol 
• 110315-43-0 (1,2-trans)-4-(1',5'-Dimethyl-4'-hexenyl)-1-methyl-4-cyclohexen-1,2-diol 

Relevant academic research and scientific papers

Terpenes and Terpene Derivatives, XXI.- Synthesis of rac-4,5-Dihydro-β-curcumene-4,5-diol

Hydrolysis of the β-curcumene monoepoxide 1 afforded the title compound 2. - A second way started from the epoxy ketone 6.Hydrolysis (-->7), formation of the THP ethers (-->8, -->9), and reaction with homoprenyllithium leads to the allylic alcohol 3.After