88073-36-3

Upstream product

• 56138-16-0 3-acetyl-2,5-diphenylfuran 
• 802294-64-0 propionic acid 
• 84302-20-5 1-((1R,4R)-1,4-Diphenyl-2,3,7-trioxa-bicyclo[2.2.1]hept-5-en-5-yl)-ethanone 
• 81396-48-7 2-aceto-1,4-diphenylbutane-1,4-dione 
• 84302-20-5 1-(1,4-Diphenyl-2,3,7-trioxa-bicyclo[2.2.1]hept-5-en-5-yl)-ethanone 

Downstream Products

• 81396-48-7 2-aceto-1,4-diphenylbutane-1,4-dione 
• 88073-34-1 3-Benzoyl-2,3-epoxy-1-phenyl-1,4-pentanedione 
• 88073-34-1 1-((2S,3R)-2,3-Dibenzoyl-oxiranyl)-ethanone 
• 56138-16-0 3-acetyl-2,5-diphenylfuran 
• 344320-91-8 (2-methyl-5-phenylfuran-3-yl)(phenyl)methanone 
• 102756-79-6 3-benzoyl-2-morpholino-1-phenyl-pentane-1,4-dione 

Relevant academic research and scientific papers

Stereoselective synthesis of α-ylidene-β-dicarbonyl compounds: A mild PhI(OAc)2-mediated dehydrogenation process

PhI(OAc)2-mediated dehydrogenation of α-alkyl-β-dicarbonyl compound has been developed to afford α-ylidene-β- dicarbonyl compounds with high stereoselectivity under mild conditions. This process provides a complementary entry to stereoselectivity for the Knoevenagel reaction.

Conjugate Reduction of 2-Butene-1,4-diones with LiAlH4-SbCl3

The reagent LiAlH4-SbCl3 was found to be more effective for a conjugate reduction of 2-butene-1,4-diones in comparison with the reagent LiAlH4-other metal halides.

Photosensitized Oxidation of Furans. Part 7. Solvent Effects in Thermal Conversion of the endo-Peroxides of Arylfurans

Thermal conversion of the endo-peroxides of the arylfurans (1) in a polar aprotic solvent leads to aroylenol esters (4) and diaroyl epoxides (3), the predominance of one over being concentration dependent.The results can be rationalized on the basis of th