94307-49-0

Upstream product

• 114-70-5 sodium phenylacetate 
• 66-99-9 β-naphthaldehyde 
• 103-82-2 phenylacetic acid 

Downstream Products

• 94305-39-2 3-naphthalen-2-yl-2-phenyl-propionic acid 
• 2039-70-5 (E)-2-styrylnaphthalene 
• 98655-16-4 2-phenyl-2,3-dihydro-1H-cyclopenta[a]naphthalen-1-one 
• 207-83-0 13H-dibenzo[a,g]fluorene 
• 100146-00-7 <2-Phenyl-4,5-benzindenyl-(3)>-essigsaeure 
• 105847-16-3 N-methyl-3-(2-naphthyl)-2-phenyl acrylohydroxamic acid 

Relevant academic research and scientific papers

Palladium-catalyzed through-space C(sp3)-H and C(sp 2)-H bond activation by 1,4-palladium migration: Efficient synthesis of [3,4]-fused oxindoles

Palladium two step: Linear anilides were converted into the title compounds in good to excellent yields through a palladium-catalyzed domino carbopalladation/1,4-palladium shift sequence. The C(sp3)-H activation involves a seven-membered pallad

Lipoxygenase inhibiting compounds

Compounds of the formula STR1 where X is selected from hydrogen, C1 to C22 alkyl or alkenyl, or an electron withdrawing group; n=0 or 1 and m=0, 1, 2 or 3; but n and m are not O simultaneously; R1 and R2 indepen

Structural Effects of the Acidity of E-α-Phenyl-β-arylacrilic Acids

The dissociation equilibrium constants of some E-α-phenyl-β-arylacrilic acids (Ar=2-pyridyl, 3-pyridyl, 4-pyridyl, 1-naphthyl, 2-naphthyl, anthracen-9-yl) have been measured in 80percent aqeous 2-methoxyethanol at 25 deg C., The pKa values of these acids, together with those of p-substituted phenyl, 2-furyl, 2-thienyl and selenophen-2-yl derivitives, have been rationalized by an equation involving separate contributions of polar, conjugative and steric effects of heterocycles.The pKa values of some E-α-phenyl-β-alkylacrilic acids (alk=methyl; ethyl; n-propyl; i-propyl; n-butyl; i-butyl) are also reported.