471931-08-5

Upstream product

• 4971-56-6 tetrahydrofuran-2,4-dione 
• 98-59-9 p-toluenesulfonyl chloride 
• 541-57-1 4-hydroxy-2(5H)-furanone 

Downstream Products

• 1575-47-9 4-phenyl-5H-furan-2-one 
• 30088-81-4 3-<4-tert.-Butyl-phenyl>-4-hydroxy-crotonsaeure-lacton 
• 30088-33-6 3-(4-methoxyphenyl)methyl-2-buten-1,4-olide 
• 476471-02-0 4-(4-fluorophenyl)-2(5H)-furanone 
• 3516-65-2 4-(4-methoxyphenyl)furan-2(5H)-one 
• 98775-10-1 4-(4-methylphenyl)furan-2(5H)-one 
• 338958-12-6 4-(4-methyl-benzyl)-5H-furan-2-one 
• 259267-02-2 4-(3,5-dimethyl-phenyl)-5H-furan-2-one 
• 7706-86-7 4-(2-methoxyphenyl)-furan-2(5H)-one 
• 26717-53-3 4-(4-chlorophenyl)furan-2(5H)-one 

Relevant academic research and scientific papers

Efficient route to 4-substituted-2(5H)-furanones, 2(1H)-quinolones, and pyrones by nickel-catalyzed cross-coupling of arenesulfonates with organozinc reagents

Nickel(II)-catalyzed cross-coupling reactions of 4-tosyl-2(1H)-quinolone, pyrone, and 2(5H)-furanone with various organozinc reagents provide an efficient and practical method for the high-yielding synthesis of 4-substituted 2(1H)-quinolones, pyrones, and 2(5H)-furanones. Copyright

Palladium-catalyzed cross-coupling reactions of 4-tosyl-2(5H)-furanone with boronic acids: A facile and efficient route to generate 4-substituted 2(5H)-furanones

An efficient and facile synthesis of 4-substituted 2(5H)-furanones using palladium catalyzed cross-coupling reactions between 4-tosyl-2(5H)-furanone and boronic acids is reported herein.