73230-88-3

Upstream product

• 73230-78-1 (-)-(4aS,6S,8aS)-6β-Acetoxy-1,2,3,4,4aα,5,6,7,8,8a-decahydro-8aβ-methyl-1-oxonaphthalene 
• 73230-82-7 <(-)-(1S,2R,4S)-4β-Acetoxy-1α-ethynyl-1β-methylcyclohex-2-yl>acetaldehyde 
• 73230-83-8 <(-)-(1R,2R,4S)-4-Acetoxy-1α-ethenyl-1-methylcyclohex-2-yl>acetaldehyde 
• 73230-80-5 (-)-(4aS,6S,8aS)-6β-Acetoxy-1,4,4aα,5,6,7,8,8a-octahydro-8aβ-methyl-1-oxonaphthalene 
• 81277-63-6 1,2,3,4,4aβ,5,6,7,8,8a-decahydro-3-hydroxy-3-<2-(4-methoxybenzocyclobutenyl)>-8aβ-methyl-1-<(methylsulfonyl)oxy>-6α-<(tetrahydropyranyl)oxy>naphthalene 
• 81339-54-0 Acetic acid (2R,4aS,8aR)-6-bromo-4a-methyl-5-oxo-decahydro-naphthalen-2-yl ester 
• 77727-30-1 (+)-(4aR,6R,8aS)-6α-acetoxy-1,4,4aβ,5,6,7,8,8a-octahydro-8aβ-methyl-1-oxonaphthalene 
• 77789-88-9 (-)-(4aR,6R,8aS)-6α-acetoxy-1,2,3,4,4aβ,5,6,7,8,8a-decahydro-8aβ-methyl-1-oxonaphthalene 
• 81277-65-8 1α-ethenyl-4α-hydroxy-2α-<2-(4-methoxybenzocyclobutenyl)-2-oxoethyl>-1β-methylcyclohexane 
• 73230-79-2 (-)-(4aS,6S,8aS)-6β-Acetoxy-2-bromo-1,2,3,4,4aα,5,6,7,8,8a-decahydro-8aβ-methyl-1-oxonaphthalene 
• 73230-81-6 (-)-(4aR,6S,8aS)-6β-Acetoxy-2,3-epoxy-1,2,3,4,4aα,5,6,7,8,8a-decahydro-8aβ-methyl-1-oxonaphthalene 
• 73284-92-1 (+)-(4aS,8aS)-1,1-(1,2-Ethylenedioxy)-1,2,3,4,4aα,5,6,7,8,8a-decahydro-8aβ-methyl-6-oxonaphthalene 
• 73230-87-2 4-Acetoxy-1-ethenyl-2-<2-(1-cyano-4-methoxybenzocyclobutenyl)-2-hydroxyethyl>-1-methylcyclohexane 
• 81339-53-9 (+)-(4aR,6R,8aS)-1,2,3,4,4aβ,5,6,7,8,8a-decahydro-1,1-(1,2-ethylenedioxy)-6-hydroxy-8aβ-methylnaphthalene 

Downstream Products

• 81277-71-6 3α,7β-bis(benzyloxy)-17-methoxy-D-homo-18-nor-5β-androsta-13,15,17-triene 
• 81277-68-1 4α-(benzyloxy)-1α-ethenyl-2α-<2-(4-methoxybenzocyclobutenyl)-2-(benzyloxy)ethyl>-1β-methylcyclohexane 

Relevant academic research and scientific papers

Asymmetric Synthesis of (-)-3β-Hydroxy-17-methoxy-D-homo-18-nor-5α-androsta-13,15,17-triene

A stereoselective synthesis of (-)-3β-hydroxy-17-methoxy-D-homo-18-nor-5α-androsta-13,15,17-triene (2), an important intermediate in the synthesis of 20-oxo-5α-Δ16-pregnen-3β-ol acetate (3), has been achieved by thermolysis of optically active