1616889-95-2

Upstream product

• 149418-41-7 3,4-dibromo-2(5H)-furanone 
• 89694-48-4 5-chloro-2-methoxyphenyl boronic acid 

Downstream Products

• 1561859-00-4 (Z)-3-bromo-5-(2-bromobenzylidene)-4-(5-chloro-2-methoxyphenyl)furan-2(5H)-one 
• 1561859-05-9 (Z)-3-bromo-4-(5-chloro-2-methoxyphenyl)-5-(3-methoxybenzylidene)furan-2(5H)-one 
• 1561859-27-5 3-bromo-5-(2-bromobenzyl)-4-(5-chloro-2-methoxyphenyl)-5-hydroxy-1-isobutylpyrrol-2-(5H)-one 
• 1561859-29-7 3-bromo-4-(5-chloro-2-methoxyphenyl)-5-hydroxy-1-isobutyl-5-(3-methoxybenzyl)pyrrol-2-(5H)-one 
• 1561859-51-5 (Z)-3-bromo-5-(2-bromobenzylidene)-4-(5-chloro-2-methoxyphenyl)-1-isobutylpyrrol-2(5H)-one 
• 1561859-74-2 (E)-3-bromo-5-(2-bromobenzylidene)-4-(5-chloro-2-methoxyphenyl)-1-isobutylpyrrol-2(5H)-one 
• 1561859-55-9 (Z)-3-bromo-4-(5-chloro-2-methoxyphenyl)-1-isobutyl-5-(3-methoxybenzylidene)pyrrol-2-(5H)-one 
• 1561859-76-4 (E)-3-bromo-4-(5-chloro-2-methoxyphenyl)-1-isobutyl-5-(3-methoxybenzylidene)pyrrol-2-(5H)-one 

Relevant academic research and scientific papers

Inhibition of Enterococcus faecalis biofilm formation by highly active lactones and lactams analogues of rubrolides

Seven β-aryl substituted γ-alkylidene-γ-lactones analogues of rubrolides were synthesized from mucobromic acid and converted through a lactamization with isobutylamine into their corresponding γ-hydroxy- γ-lactams (76-85%). These lactams were converted in