92206-82-1

Upstream product

• 6559-91-7 (+/-)-4'-O-demethyl-1-epipodophyllotoxin 
• 79-04-9 chloroacetyl chloride 
• 477-47-4 (+/-)-podophyllotoxin 

Downstream Products

• 112146-51-7 1-O-(2-benzyloxycarbonylamido-3-chloroacetyl-2-deoxy-4:6-O-ethylidene-β-D-glucopyranosyl)-<(-)-4'-O-chloroacetyl-1-epipodophyllotoxin> 
• 112146-51-7 1-O-(2-benzyloxycarbonylamido-3-chloroacetyl-2-deoxy-4:6-O-ethylidene-β-D-glucopyranosyl)-<(+)-4'-O-chloroacetyl-1-epipodophyllotoxin> 
• 112146-51-7 C₄₁H₄₁Cl₂NO₁₆ 
• 112146-51-7 C₄₁H₄₁Cl₂NO₁₆ 
• 105655-99-0 1-O-(2-deoxy-2-dimethylamino-β-L-glucopyranosyl)-<(+)-1-epipodophyllotoxin> 
• 105655-99-0 1-O-(2-deoxy-2-dimethylamino-β-D-glucopyranosyl)-<(+)-1-epipodophyllotoxin> 
• 105655-99-0 1-O-(2-deoxy-2-dimethylamino-β-L-glucopyranosyl)-<(-)-1-epipodophyllotoxin> 
• 105655-99-0 1-O-(2-deoxy-2-dimethylamino-β-D-glucopyranosyl)-<(-)-1-epipodophyllotoxin> 
• 112317-52-9 1-O-(2-amino-2-deoxy-β-L-glucopyranosyl)-<(+)-1-epipodophyllotoxin> 
• 112318-79-3 1-O-(2-amino-2-deoxy-β-D-glucopyranosyl)-<(+)-1-epipodophyllotoxin> 
• 112246-51-2 1-O-(2-amino-2-deoxy-β-L-glucopyranosyl)-<(-)-1-epipodophyllotoxin> 
• 131118-85-9 {(2S,4aS,6S,7S,8S,8aR)-8-Hydroxy-6-[(5R,5aS,8aS,9S)-9-(4-hydroxy-3,5-dimethoxy-phenyl)-8-oxo-5,5a,6,8,8a,9-hexahydro-furo[3',4':6,7]naphtho[2,3-d][1,3]dioxol-5-yloxy]-2-methyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl}-carbamic acid benzyl ester 
• 131118-85-9 {(2R,4aR,6R,7R,8R,8aS)-8-Hydroxy-6-[(5R,5aS,8aS,9S)-9-(4-hydroxy-3,5-dimethoxy-phenyl)-8-oxo-5,5a,6,8,8a,9-hexahydro-furo[3',4':6,7]naphtho[2,3-d][1,3]dioxol-5-yloxy]-2-methyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl}-carbamic acid benzyl ester 
• 131118-85-9 {(2S,4aS,6S,7S,8S,8aR)-8-Hydroxy-6-[(5S,5aR,8aR,9R)-9-(4-hydroxy-3,5-dimethoxy-phenyl)-8-oxo-5,5a,6,8,8a,9-hexahydro-furo[3',4':6,7]naphtho[2,3-d][1,3]dioxol-5-yloxy]-2-methyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl}-carbamic acid benzyl ester 

Relevant academic research and scientific papers

Syntheses of All Four Possible Diastereomers of Etoposide and Its Aminoglycosidic Analogues via Optical Resolution of (+/-)-Podophyllotoxin by Glycosidation with D- and L-Sugars

Syntheses of all four possible diastereomers of etoposide and its aminoglycosidic analogues have been achieved via optical resolution of (+/-)-podophyllotoxin by glycosidation with D- and L-sugars.