70546-62-2

Upstream product

• 115819-65-3 ((4aR,8aS)-4,4,7-Trimethyl-3-oxo-1,2,3,4,4a,5,6,8a-octahydro-naphthalen-2-yl)-acetic acid ethyl ester 
• 115819-73-3 ((4aR,8aS)-4,4,7-Trimethyl-3-oxo-1,2,3,4,4a,5,6,8a-octahydro-naphthalen-2-yl)-acetic acid 
• 115819-64-2 (4aS,8aR)-1,1,6-Trimethyl-3,4,4a,7,8,8a-hexahydro-1H-naphthalen-2-one 
• 61530-97-0 (4aS,8aR)-6-Methyl-3,4,4a,7,8,8a-hexahydro-1H-naphthalen-2-one 
• 178324-30-6 1-Furan-3-yl-4,8-dimethyl-non-7-en-2-yn-4-ol 
• 178324-27-1 (E)-1-Furan-3-yl-4,8-dimethyl-nona-2,7-dien-4-ol 
• 115819-66-4 (4aS,8aR)-6,9,9-Trimethyl-4a,7,8,8a,9,9a-hexahydro-4H-naphtho[2,3-b]furan-2-one 

Relevant academic research and scientific papers

Synthesis of (±)-furodizinin and (±)-furodizin

The racemic forms of natural furanoterpenoids, (±)-furodizinin and (±)-furodizin, were synthesized by cationic cyclization of the α-or β-furylmethyl derivatives of linalool, geraniol, and nerol.

Total Synthesis of (+/-)-Furodysin and (+/-)-Furodysinin

Furodysin and furodysinin, marine origin furanosesquiterpenes having a unique carbocyclic ring system, have been first synthesized as racemic forms from a cis-decalone derivative.