390361-89-4

Upstream product

• 345895-23-0 (2-octyloxy-hex-5-enyl)-benzene 
• 1826-67-1 vinyl magnesium bromide 
• 451503-08-5 4-octyloxy-5-phenyl-pentanal 
• 5729-65-7 1-phenyl-5-hexene-2-ol 
• 4436-24-2 1,2-epoxy-3-phenylpropane 

Downstream Products

• 390361-90-7 (E)-8-octyloxy-9-phenyl-non-4-enoic acid ethyl ester 
• 390361-91-8 (E)-8-octyloxy-9-phenyl-non-4-en-1-ol 
• 451503-10-9 (2E,6E)-10-Octyloxy-11-phenyl-undeca-2,6-dien-1-ol 
• 873925-45-2 (2E,6E)-10-Octyloxy-11-phenyl-undeca-2,6-dienoic acid ethyl ester 
• 451503-09-6 [(5E,9E)-11-(1-Ethoxy-ethoxy)-2-octyloxy-undeca-5,9-dienyl]-benzene 
• 390361-92-9 (E)-2-(8-octyloxy-9-phenyl-non-4-enyloxy)-tetrahydropyran 
• 873925-46-3 [(2S,3S)-3-((E)-7-Octyloxy-8-phenyl-oct-3-enyl)-oxiranyl]-methanol 
• 873925-47-4 (2S,3S)-2-(1-Ethoxy-ethoxymethyl)-3-((E)-7-octyloxy-8-phenyl-oct-3-enyl)-oxirane 
• 873925-34-9 C₂₉H₄₈O₅ 
• 873925-33-8 C₂₉H₄₈O₅ 
• 390361-95-2 2-{3-[3-(3-octyloxy-4-phenyl-butyl)oxiranyl]propoxy}-tetrahydropyran 

Relevant academic research and scientific papers

Electron transfer initiated heterogenerative cascade cyclizations: Polyether synthesis under nonacidic conditions

(Matrix presented) Single-electron oxidation has been employed to initiate heterogenerative cascade cyclization reactions that form polyether compounds under essentially neutral conditions. The reactions proceed through mesolytic benzylic carbon-carbon bo

Aerobic organocatalytic photoinitiated arene oxidations: Application to electron transfer initiated cyclization reactions

(matrix presented) Electron transfer initiated oxidative cyclization reactions can be effected by catalytic amounts of N-methylquinolinium hexafluorophosphate through photoirradiation in the presence of dioxygen. Solid sodium thiosulfate serves as an effe