87961-41-9

Usage

InChI:InChI=1/C12H12O5/c13-9(2-1-3-12(14)15)8-4-5-10-11(6-8)17-7-16-10/h4-6H,1-3,7H2,(H,14,15)

Upstream product

• 108-55-4 glutaric anhydride, 
• 274-09-9 Methylenedioxybenzene 
• 95849-53-9 1-(3,4-methylenedioxyphenyl)cyclopentene 
• 63765-10-6 (1S,2R)-2-Benzo[1,3]dioxol-5-yl-cyclohexanol 
• 214334-34-6 1,1,6,6-tetramethoxy-1,6-bis(3,4-methylenedioxyphenyl)hexane 
• 214334-35-7 1,6-bis(3,4-methylenedioxyphenyl)hexane-1,6-diol 
• 6268-56-0 1,6-bis(3,4-methylenedioxyphenyl)hexane-1,6-dione 
• 120-57-0 piperonal 

Downstream Products

• 91-89-4 6-(benzo[1,3]dioxol-5-yl)pyran-2-one 

Relevant academic research and scientific papers

Visible-Light-Promoted Metal-Free Aerobic Oxidation of Primary Amines to Acids and Lactones

A unique metal-free aerobic oxidation of primary amines via visible light photocatalytic double carbon–carbon bonds cleavage and multi carbon–hydrogen bonds oxidation was observed. Aerobic oxidation of primary amines could be controlled to afford acids by using dioxane with 18 W CFL, and lactones by using DMF with 8 W green LEDs, respectively. A plausible mechanism was proposed based on control experiments. This observation showed direct evidences for the fragmentation in the aerobic oxidation of aliphatic primary amines.

Lewis Acid-Promoted Disproportionation Reaction of Aromatic Vinyl Ethers and Acetals and Its Application to the Synthesis of Paracotoin

Aromatic vinyl ethers and acetals underwent a novel addition-fragmentation reaction affording olefins and esters in the presence of a Lewis acid. This reaction was applied to intramolecular cyclization reaction, giving five or six membered ring compounds in good yields. Paracotoin, an intermediate in the biosynthesis of shikimic acid, was synthesized using this cyclization reaction as the key step.