672931-65-6

Upstream product

• 358-23-6 trifluoromethylsulfonic anhydride 
• 139386-27-9 ethyl 3-(2-hydroxy-4-methoxyphenyl)-(E)-2-propenoate 
• 531-59-9 7-methoxycoumarin 

Downstream Products

• 1417997-78-4 C₂₂H₂₀O₃ 
• 1417997-80-8 C₂₄H₂₂O₄ 
• 1417997-81-9 C₂₅H₂₂O₄ 
• 1417997-82-0 C₂₄H₂₀O₄ 
• 1417997-85-3 C₂₀H₁₆O₃ 
• 1417997-87-5 C₂₂H₁₈O₄ 
• 1417997-88-6 C₂₃H₁₈O₄ 
• 1417997-89-7 C₂₂H₁₆O₄ 
• 1417997-92-2 (E)-N-hydroxy-4-methoxy-2-(naphthalen-1-yl)cinnamamide 
• 1417997-93-3 (E)-N-hydroxy-4-methoxy-2-(biphenyl-4-yl)cinnamamide 
• 1417997-94-4 (E)-N-hydroxy-4-methoxy-2-(4-phenoxyphenyl)cinnamamide 
• 1417997-95-5 (E)-N-hydroxy-4-methoxy-2-(4-benzoylphenyl)cinnamamide 
• 1417997-96-6 (E)-N-hydroxy-4-methoxy-2-(dibenzofuran-4-yl)cinnamamide 

Relevant academic research and scientific papers

An efficient route from coumarins to highly functionalized N-phenyl-2-quinolinones via Buchwald-Hartwig amination

Multiple substituted N-phenyl-2-quinolinones were obtained in a convenient four-step route from a variety of commercially available coumarins, utilizing customised Buchwald-Hartwig amination protocols for the key reaction. Whereas simple aminolysis of cou

Synthesis and Biological Evaluation of ortho-Aryl N-Hydroxycinnamides as Potent Histone Deacetylase (HDAC) 8 Isoform-Selective Inhibitors

Histone deacetylases (HDACs) are a family of enzymes that play a crucial role in biological process and diseases. In contrast to other isozymes, HDAC8 is uniquely incapable of histone acetylation. In order to delineate its physiological function, we devel