27063-62-3

Upstream product

• 123-11-5 4-methoxy-benzaldehyde 
• 74076-63-4 2-(4-methoxyphenyl)-4,7-dihydro-1,3-dioxepine 

Downstream Products

• 119649-30-8 2-Benzyloxy-5-(4-methoxy-benzyloxy)-pentanal 
• 119649-29-5 1-(4-Benzyloxy-hex-5-enyloxymethyl)-4-methoxy-benzene 
• 154476-70-7 6-(4-methoxybenzyloxy)hex-1-en-3-ol 
• 119649-27-3 4-((4-methoxybenzyl)oxy)butanal 
• 119649-45-5 4-(p-methoxybenzyloxy)butan-1-ol 

Relevant academic research and scientific papers

Lewis Acid-Catalyzed Vinyl Acetal Rearrangement of 4,5-Dihydro-1,3-dioxepines: Stereoselective Synthesis of cis- And trans-2,3-Disubstituted Tetrahydrofurans

Lewis acid-catalyzed rearrangements of 4,5-dihydro-1,3-dioxepines have been investigated. Rearrangement of vinyl acetals under a variety of conditions resulted in cis- and trans-2,3-disubstituted tetrahydrofuran derivatives in a highly stereoselective man