112890-48-9

Upstream product

• 42172-62-3 (Z)-3-(4-methoxyphenyl)-2-(4-nitrophenyl)acrylonitrile 
• 6582-07-6 3-(4-methoxy-phenyl)-2-(4-nitro-phenyl)-acrylonitrile 

Downstream Products

• 112890-52-5 2-Cyano-5-(p-methoxyphenyl)-2-(p-nitrophenyl)tetrahydrofuran-3,4-dicarboxylic anhydride 
• 129913-45-7 (1S,3R,3aS,6aS)-3-(4-Methoxy-phenyl)-1-(4-nitro-phenyl)-4-oxo-tetrahydro-furo[3,4-c]furan-1-carbonitrile 
• 129913-44-6 (1S,3R,3aR,6aR)-3-(4-Methoxy-phenyl)-1-(4-nitro-phenyl)-6-oxo-tetrahydro-furo[3,4-c]furan-1-carbonitrile 
• 112890-61-6 Methyl 2-cyano-5-(p-methoxyphenyl)-2-(p-nitrophenyl)tetrahydrofuran-4-carboxylate 
• 112890-60-5 Methyl 2-cyano-5-(p-methoxyphenyl)-2-(p-nitrophenyl)tetrahydrofuran-3-carboxylate 

Relevant academic research and scientific papers

Synthetic Studies on O-Heterocycles via Cycloadditions. Part 3. Regiochemical and Mechanistic Questions in Reactions of Polarised Diaryl Carbonyl Ylides

The unsymmetrical diaryloxiranes (9), (24), (25), and (26) undergo smooth cycloaddition with electron-deficient olefins under thermal or photochemical initiation, apparently via polarised carbonyl ylide intermediates.With unsymmetrical dipolarophiles the

Polarised Diaryl Carbonyl Ylids : The Specificity of Additions to Unsymmetric Dipolarophiles

'Push-pull' carbonyl ylids derived thermally or photochemically from oxiranes (14-16) undergo stereospecific, but uncharacteristically non-regioselective, cycloadditions with unsymmetrical electron-deficient dipolarophiles.