438627-86-2

Upstream product

• 438627-73-7 (3aS,4S,6R,6aR)-6-(tert-Butyl-dimethyl-silanyloxy)-4-(3,4-dimethoxy-phenyl)-2,2-dimethyl-tetrahydro-cyclopenta[1,3]dioxol-4-ol 
• 288269-05-6 (3aS,6R,6aR)-6-(tert-Butyl-dimethyl-silanyloxy)-2,2-dimethyl-tetrahydro-cyclopenta[1,3]dioxol-4-one 
• 438627-84-0 2-[(1S,2R)-1-(3,4-Dimethoxy-phenyl)-2,3-dihydroxy-3-methyl-cyclopentyl]-N-methyl-acetamide 
• 438627-79-3 2-[4-(3,4-dimethoxy-phenyl)-2,2-dimethyl-tetrahydro-cyclopenta[1,3]dioxol-4-yl]-N,N-dimethyl-acetamide 
• 438627-78-2 2-[4-(3,4-dimethoxy-phenyl)-2,2-dimethyl-4,6a-dihydro-3aH-cyclopenta[1,3]dioxol-4-yl]-N,N-dimethyl-acetamide 
• 438627-74-8 (3aS,4S,6R,6aS)-4-(3,4-Dimethoxy-phenyl)-2,2-dimethyl-tetrahydro-cyclopenta[1,3]dioxole-4,6-diol 
• 438627-75-9 (3aR,6S,6aS)-6-(3,4-Dimethoxy-phenyl)-6-hydroxy-2,2-dimethyl-tetrahydro-cyclopenta[1,3]dioxol-4-one 
• 438627-83-9 (3aS,6aR)-3a-(3,4-Dimethoxy-phenyl)-6-hydroxy-6-methyl-hexahydro-cyclopenta[b]furan-2-one 
• 438627-80-6 (3aS,6S,6aR)-3a-(3,4-Dimethoxy-phenyl)-6-hydroxy-hexahydro-cyclopenta[b]furan-2-one 
• 438627-81-7 (3aS,6aR)-3a-(3,4-Dimethoxy-phenyl)-tetrahydro-cyclopenta[b]furan-2,6-dione 
• 438627-77-1 (3aS,4S,6aR)-6-(3,4-Dimethoxy-phenyl)-2,2-dimethyl-4,6a-dihydro-3aH-cyclopenta[1,3]dioxol-4-ol 
• 438627-76-0 (3aR,6aR)-6-(3,4-Dimethoxy-phenyl)-2,2-dimethyl-3a,6a-dihydro-cyclopenta[1,3]dioxol-4-one 
• 2859-78-1 4-Bromoveratrole 

Downstream Products

• 438627-88-4 {2-[(1S,2R)-1-(3,4-Dimethoxy-phenyl)-2,3-dihydroxy-3-methyl-cyclopentyl]-ethyl}-methyl-carbamic acid methyl ester 
• 216005-93-5 {2-[(R)-1-(3,4-Dimethoxy-phenyl)-4-oxo-cyclohex-2-enyl]-ethyl}-methyl-carbamic acid methyl ester 
• 438627-90-8 [(S)-3-(3,4-Dimethoxy-phenyl)-3-formyl-6-oxo-heptyl]-methyl-carbamic acid methyl ester 

Relevant academic research and scientific papers

A new enantioselective route to the Sceletium alkaloids via a cyclopentanone-cyclohexenone transformation

An enantioselective route to the Sceletium alkaloids has been developed using the 2,3,4-trioxycyclopentanone chiral building block by carrying out its conversion into a 4,4-disubstituted cyclohexenone derivative.