1158649-25-2

Upstream product

• 1158649-28-5 methyl (Z)-2-(3-hydroxy-4-(4-methoxyphenyl)-5-oxofuran-2(5H)-ylidene)acetate 

Downstream Products

• 1158649-32-1 methyl (E)-2-(3-hydroxy-4-(4-methoxyphenyl)-5-oxofuran-2(5H)-ylidene)-2-(2-(trifluoromethyl)phenyl)acetate 
• 481-64-1 (E)-4-hydroxy-5-(α-methoxycarbonylbenzylidene)-3-(4-methoxyphenyl)furan-2(5H)-one 
• 1158649-30-9 methyl (E)-2-(4-chlorophenyl)-2-(3-hydroxy-4-(4-methoxyphenyl)-5-oxofuran-2(5H)-ylidene)acetate 
• 1158649-34-3 methyl (E)-2-(3-hydroxy-4-(4-methoxyphenyl)-5-oxofuran-2(5H)-ylidene)-2-(3-thienyl)acetate 
• 1158649-31-0 methyl (E)-2-(3-hydroxy-4-(4-methoxyphenyl)-5-oxofuran-2(5H)-ylidene)-2-(3-(trifluoromethyl)phenyl)acetate 
• 1158649-29-6 methyl (E)-2-(3-hydroxy-4-(4-methoxyphenyl)-5-oxofuran-2(5H)-ylidene)-2-(3-hydroxyphenyl)acetate 

Relevant academic research and scientific papers

Synthesis and antioxidant properties of pulvinic acids analogues

The synthesis of three types of pulvinic acid analogues, using a diversity-oriented strategy starting from a single compound, dimethyl l-tartrate, is described. Lacey-Dieckmann condensation, alcohol dehydration and Suzuki-Miyaura cross-couplings were empl

Synthesis of vulpinic acids from dimethyl tartrate

A series of vulpinic acids differing by the aryl or heteroaryl groups placed in the ester α-position were prepared by Suzuki-Miyaura cross-coupling involving a common iodide and the corresponding aryl boronates. The preparation of the iodide precursor fro