223103-60-4

Upstream product

• 23074-59-1 3-isobutoxycyclohex-2-en-1-one 
• 78878-05-4 1-iodo-3-(tert-butyldimethylsilyloxy)propane 

Downstream Products

• 223103-66-0 3-(3-methyl-allyl)-4-(4-phenylsulfanyl-hexa-3(E),5-dienyl)-2-cyclohexen-1-one 
• 223103-62-6 3-isobutoxy-6-(4-phenylsulfanyl-hexa-3(E),5-dienyl)-2-cyclohexen-1-one 
• 222023-21-4 3-Isobutoxy-1-methyl-6-((Z)-4-phenylsulfanyl-hexa-3,5-dienyl)-cyclohex-2-enol 
• 222023-27-0 3-Isobutoxy-6-((Z)-4-phenylsulfanyl-hexa-3,5-dienyl)-cyclohex-2-enone 
• 222023-26-9 3-(4-isobutoxy-2-oxo-cyclohexen-3-enyl)-propionaldehyde 
• 223103-61-5 6-(3-hydroxy-propyl)-3-isobutoxy-2-cyclohexen-1-one 

Relevant academic research and scientific papers

Functionalized carbocyclic rings via intramolecular Diels-Alder reactions of in situ-generated, γ substituted, heteroatom-stabilized allyl cations in acidic polar media

The synthesis of highly structured carbocyclic ring systems possessing quaternary carbon atoms has been realized via intramolecular Diels-Alder reactions of in situ-generated, γ substituted, heteroatom-stabilized allyl cations in acidic polar media.