75101-87-0

Upstream product

• 76886-74-3 C₂₄H₂₂O₁₀ 
• 120-57-0 piperonal 
• 74879-22-4 6-bromobenzo-1,3-dioxole-5-carboxaldehyde dimethyl acetal 
• 86-81-7 3,4,5-trimethoxy-benzaldehyde 
• 74879-25-7 -3,4-methylenedioxybenzaldehyde dimethyl acetal 
• 75101-87-0 dimethyl 1,4-epoxy-1,2,3,4-tetrahydro-6,7-(methylenedioxy)-1-(1,2-cis)-(3',4',5'-trimethoxyphenyl)-2,3-cis-naphthalenedicarboxylate 

Downstream Products

• 42123-26-2 dimethyl 6,7-methylenedioxy-1-(3',4',5'-trimethoxyphenyl)naphthalene-2,3-dicarboxylate 
• 122763-44-4 dimethyl 4-(3,4-trans)-hydroxy-6,7-(methylenedioxy)-1-(3',4',5'-trimethoxyphenyl)-3,4-dihydronaphthalene-2,3-dicarboxylate 
• 86301-75-9 dimethyl 4-(3,4-trans)-hydroxy-6,7-(methylenedioxy)-1-(1,2-cis)-(3',4',5'-trimethoxyphenyl)-1,2,3,4-tetrahydronaphthalene-2,3-cis-dicarboxylate 
• 122763-45-5 dimethyl 4-(3,4-trans)-hydroxy-6,7-(methylenedioxy)-1-(3',4',5'-trimethoxyphenyl)-2,3,4,4a,5,6,7,8-octahydro-2-naphthalene-2,3-cis-dicarboxylate 
• 42123-24-0 dimethyl 4-hydroxy-6,7-methylenedioxy-1-(3',4',5'-trimethoxyphenyl)naphthalene-2,3-dicarboxylate 
• 75101-87-0 dimethyl 1,4-epoxy-1,2,3,4-tetrahydro-6,7-(methylenedioxy)-1-(1,2-cis)-(3',4',5'-trimethoxyphenyl)-2,3-trans-naphthalenedicarboxylate 
• 477-67-8 isopodophyllic acid 
• 122763-50-2 methyl 3-(hydroxymethyl)-6,7-(methylenedioxy)-1-(1,2-cis)-(3',4',5'-trimethoxyphenyl)-1,2-dihydronaphthalene-2-carboxylate 
• 79289-93-3 epipodophyllic acid 4,11-acetonide 
• 79305-58-1 methyl epipodophyllate 4,11-acetonide 
• 477-51-0 deoxypicropodophyllotoxin 
• 477-47-4 (+/-)-epi-picropodophyllin 
• 477-47-4 (+/-)-isopodophyllotoxin 
• 477-47-4 (+/-)-epipodophyllotoxin 

Relevant academic research and scientific papers

Comprehensive Synthetic Route to Eight Diastereomeric Podophyllum Lignans

An oxabicyclo compound, 9, prepared in 47percent yield through an isobenzofuran intermediate was converted with excellent regio- and stereocontrol to eight (+/-)-lignan lactones of the podophyllotoxin series.One of the eight, epiisopicropodophyllin, 36, t

A Stereo- and Regiocontrolled Synthesis of Podophyllum Lignans

A Diels-Alder adduct of an isobenzofuran (generated in situ) and dimethyl acetylenedicarboxylate is converted by a series of controlled reductions and isomerizations to the lignans deoxy- and isodeoxypodophyllotoxin in seven stages.