473-66-5

Upstream product

• 13040-03-4 (+)-cis-verbenol 

Downstream Products

• 136309-69-8 N-p-tolyl-cis-pinane-4-amine 
• 136309-70-1 N-p-methoxyphenyl-cis-pinane-4-imine 
• 136309-75-6 4-phenyloamino-2,6,6-trimethylbicyclo<3.1.1>heptane 
• 80-57-9 (+/-)-2,6,6-trimethylbicyclo[3.1.1]hept-2-en-4-one 
• 105497-89-0 (4R,5R)-4-Isopropyl-5-methyl-cyclohex-2-enone 
• 105497-90-3 (4R,5R)-5-methyl-4-(2-propyl)cyclohex-2-enone 
• 77510-81-7 (1R-cis)-(+)-2,2-dimethyl-3-(1-methylethenyl)cyclobutanemethanol acetate 
• 28465-10-3 (+)-(1R)-cis-2,2-dimethyl-3-isopropenylcyclobutanemethanol acetate 
• 473-55-2 trans-pinane 
• 1292847-75-6 (2S,4S,4aR,8R,8aR)-3,4,4a,5,8,8a-hexahydro-4,7-dimethyl-2-phenyl-2H-chromene-4,8-diol 
• 935670-67-0 (1R,2R,6S)-3-methyl-6-(1-methylethenyl)cyclohex-3-ene-1,2-diol 

Relevant academic research and scientific papers

Enantioselectivity in the Biotransformation of Mono- and Bicyclic Monoterpenoids with the Cultured Cells of Nicotiana tabacum

The biotransformation of the enantiomeric pairs of p-menthane and bicyclo and heptane derivatives with the cultured cells of Nicotiana tabacum was investigated.It was found that (i) the cultured cells discriminate the enantiomers of p-menthan-2-ol and bicycloheptan-2-ol and bicycloheptan-3-ol derivatives, and enantioselectively convert these alcohols to the corresponding ketones, (ii) the cells reduce the carbonyl group of p-methan-2-one derivatives to a high extent, but not that of p-menthan-3-ones, and (iii) the cells discriminate the enantiomers of bicyclohept-2-en-4-one (verbenone) and enantioselectively reduce the C-C double bond of the (1S,5S)-enantiomer.