451503-08-5

Upstream product

• 5729-65-7 1-phenyl-5-hexene-2-ol 
• 345895-23-0 (2-octyloxy-hex-5-enyl)-benzene 

Downstream Products

• 390361-89-4 6-octyloxy-7-phenyl-hept-1-en-3-ol 
• 873925-47-4 (2S,3S)-2-(1-Ethoxy-ethoxymethyl)-3-((E)-7-octyloxy-8-phenyl-oct-3-enyl)-oxirane 
• 873925-46-3 [(2S,3S)-3-((E)-7-Octyloxy-8-phenyl-oct-3-enyl)-oxiranyl]-methanol 
• 390361-90-7 (E)-8-octyloxy-9-phenyl-non-4-enoic acid ethyl ester 
• 873925-33-8 C₂₉H₄₈O₅ 
• 873925-34-9 C₂₉H₄₈O₅ 
• 390361-92-9 (E)-2-(8-octyloxy-9-phenyl-non-4-enyloxy)-tetrahydropyran 
• 451503-09-6 [(5E,9E)-11-(1-Ethoxy-ethoxy)-2-octyloxy-undeca-5,9-dienyl]-benzene 
• 873925-45-2 (2E,6E)-10-Octyloxy-11-phenyl-undeca-2,6-dienoic acid ethyl ester 
• 451503-10-9 (2E,6E)-10-Octyloxy-11-phenyl-undeca-2,6-dien-1-ol 
• 390361-91-8 (E)-8-octyloxy-9-phenyl-non-4-en-1-ol 

Relevant academic research and scientific papers

Oxidatively generated electrophiles as initiators of epoxide cascade cyclization processes

Oxidatively generated oxocarbenium ions are shown to be effective promoters of polyepoxide cascade cyclization reactions to form polyether compounds. The reaction conditions are neutral, ensuring that background acid-mediated processes are not operative a

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