61247-11-8

Upstream product

• 78420-33-4 (4aS)-4a-methyl-trans-octahydro-naphthalen-2-one 
• 61247-08-3 2,8aα-Dimethyl-trans-Δ²-octalon-(5) 
• 61195-20-8 2,8aα-Dimethyl-5α-(1-methyl-2-hydroxy-propyloxy)-trans-Δ²-octalin 
• 938-07-8 trans-10-methyldecal-2-one 
• 21789-56-0 (+/-)-4a-methyl-(4ar,8at)-1,2,3,4,4a,5,8,8a-octahydro-naphthalene 
• 1197-95-1 (+/-)-3-Oxo-4a-methyl-trans-decalin 
• 78-94-4 methyl vinyl ketone 
• 77748-80-2 1-((4aR,8aR)-3-Hydroxy-8a-methyl-1,4,4a,5,6,7,8,8a-octahydro-naphthalen-2-yl)-ethanone 
• 826-56-2 4a-methyl-4,4a,5,6,7,8-hexahydro-3H-naphthalen-2-one 
• 1197-95-1 cis-9-Methyl-decalon-(2) 
• 938-06-7 (+-)-4a-methyl-cis-octahydro-naphthalen-2-one 
• 1196-55-0 4,4a,5,6,7,8-hexahydronaphthalen-2(3H)-one 
• 13482-23-0 4-methoxycyclohexanone 
• 2547-28-6 trans-6-methylbicyclo<3.3.0>decan-3α-ol 

Downstream Products

• 13351-29-6 trans-8-Methylhydrindan-2-on 
• 13351-29-6 cis-2H-1,3,3a,4,5,6,7,7a-octahydro-7a-methyl-2-indenone 
• 13351-29-6 trans-Octahydro-3a-methyl-2H-inden-2-one 

Relevant academic research and scientific papers

Stereochemical Studies. VIII. Further Studies of Stereochemical Effects on the Course of Oxidation of α-Acyloctahydronaphthalenones

trans-Fused octahydroindene-1- and -2-carboxylic acids are formed stereoselectively on oxidation of α-acyl derivatives of trans-fused octahydronaphthalen-1(2H)- and 2(1H)-ones by hydrogen peroxide.