10064-26-3

Usage

Uses

The provided materials do not specify any particular uses for (4aS,10aS)-1,1,4a-Trimethyl-6-methoxy-7-isopropyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene. However, given its complex structure and the presence of various functional groups, it is plausible that (4aS,10aS)-1,1,4a-Trimethyl-6-methoxy-7-isopropyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene could have potential applications in various fields such as pharmaceuticals, materials science, or as an intermediate in the synthesis of other organic compounds. Further research and development would be necessary to explore and confirm its specific uses.

Upstream product

• 4698-08-2 (E)-geranic acid 
• 5389-87-7 1-chloro-3,7-dimethylocta-2,6-diene 

Downstream Products

• 514-62-5 ferruginol 
• 511-05-7 sugiol 
• 140923-35-9 (+/-)-6-hydroxy-5,6-dehydrosugiol 
• 64158-71-0 (+/-)-12-Benzoyloxyabieta-8,11,13-trien-6β,11-diol 
• 514-62-5 (+/-)-ferruginol 
• 511-05-7 (+)-sugiol 
• 55898-07-2 6α-hydroxy-7-oxoferruginol 
• 140923-35-9 6-Hydroxy-5,6-dehydrosugiol 
• 79433-43-5 2<2(2-isopropyl-1,4-benzoquinone-5-yl)-2,6,6-trimethylcyclohexyl> acetic acid 
• 79433-46-8 ((1S,2S)-4',5'-Dibromo-4'-isopropyl-1,3,3-trimethyl-3',6'-dioxo-bicyclohexyl-1'-en-2-yl)-acetic acid 
• 79433-45-7 2<2(2-bromo-3-isopropyl-1,4-benzoquinone-6-yl)-2,6,6-trimethylcyclohexyl> acetic acid 
• 79433-44-6 2<2(2-hydroxy-3-isopropyl-1,4-benzoquinone-6-yl)-2,6,6-trimethylcyclohexyl> acetic acid 
• 21764-42-1 5,6-dehydrosugiol 
• 337909-73-6 Benzoic acid (4bS,8aS)-4-acetoxy-9-chloro-2-isopropyl-4b,8,8-trimethyl-10-oxo-4b,5,6,7,8,8a,9,10-octahydro-phenanthren-3-yl ester 

Relevant academic research and scientific papers

Synthesis of (+)- and (-)-ferruginol via asymmetric cyclization of a polyene

Stereoselectivity of modified polyenes which have a terminal benzene ring was found to be dependent on the size of substituent on the adjacent asymmetric carbon to the terminal benzene ring of the polyenes. (R)-(+)-2′-Hydroxy-1,1′-binaphthyl-2-yl(2R)-2-(4-methoxyphenyl)-5,9- dimethyldeca-4,8-dienoate gave(R)-(+)-2′-hydroxy-1,1′-binaphthyl-2-yl (4aS,9 R, 10aS)-1,2,3,4,4a,9,10,10a-octahydro-6-methoxy-1,1,4a-trimethylphenanthene-9- carboxylate stereoselectively by treatment with BF3-Et2O in nitromethane. The products were elaborated to (+)-ferruginol 1. (-)-Ferruginol 2 and (±)-ferruginol 3 were also synthesized via a similar synthetic route. The Royal Society of Chemistry 2000.

Stereoselective synthesis of (+)-ferruginyl methyl ether and (+)-sugiyl methyl ether

A facile stereoselective synthetic procedure to (+)-ferruginyl methyl ether and (+)-sugiyl methyl ether has been developed with high stereoselectivity and overall yield.

Stereoselective synthesis of (-)-6,7-dehydroferruginyl methyl ether

A stereoselective synthetic route to (-)-6,7-dehydroferruginyl methyl ether was developed from (S)-(-)-α-cyclocitral. Copyright (C) 2000 Elsevier Science Ltd.