3293-45-6

Upstream product

• 13720-37-1 dihydro-α-ionol 
• 108-24-7 acetic anhydride 
• 31499-72-6 7,8-dihydro-α-ionone 
• 108-05-4 vinyl acetate 
• 127-41-3 alpha-ionone 

Downstream Products

• 68479-99-2 2-Acetoxy-4-(2',2'-dimethyl-6'-methyliden-1'-cyclohexyl)butan 
• 13720-12-2 4-(2',2'-Dimethyl-6'-methylidenecyclohexyl)butan-2-one 
• 129966-84-3 3-(3-hydroxy-butyl)-2,4,4-trimethyl-cyclohexanone 
• 35316-49-5 2-((E)-5-Bromo-3-methyl-pent-3-enyl)-1,1-dimethyl-3-methylene-cyclohexane 
• 35316-47-3 trans-8-Monocyclofarnesol 
• 23917-09-1 Presiccanochromene-A 
• 35316-45-1 (E)-5-(2,2-Dimethyl-6-methylene-cyclohexyl)-3-methyl-pent-2-enoic acid ethyl ester 
• 347852-13-5 7,8-dihydro-α-ionol 
• 41678-32-4 (-)-dihydroedulan II 
• 137937-64-5 (1R,1'R*,2'R*,3'S*)-3-(2',3'-epoxy-2',6',6'-trimethyl-2'-cyclohexenyl)-1-methylpropyl p-toluenesulfonate 
• 137937-65-6 (1R,1'R*,2'R*,3'R*)-3-(2',3'-dihydroxy-2',6',6'-trimethyl-2'-cyclohexenyl)-1-methylpropyl p-toluenesulfonate 
• 14554-14-4 (1R,1'RS)-1-methyl-3-(2',6',6'-trimethyl-2'-cyclohexenyl)propyl p-toluenesulfonate 

Relevant academic research and scientific papers

A Synthetic Study of (-)-Dihydroedulan II and Related Compounds

(-)-Dihydroedulan II and related compounds were synthesized from (2R,1'RS)-dihydro-α-ionol, which was prepared by lipase-catalyzed enantioselective transesterification of the corresponding diastereomeric mixture as the key-step.Fungal allylic oxidation of (-)-dihydroedulan II worked well to afford a corresponding alcohol as well as (+)-dihydroedulan-8-one.