39170-33-7

Upstream product

• 36710-32-4 1-(5-(4-bromophenyl)furan-2-yl)ethanone 

Downstream Products

• 53174-12-2 2-[5-(4-bromo-phenyl)-furan-2-yl]-imidazo[1,2-a]pyridine 
• 42142-96-1 4-[5-(4-bromo-phenyl)-furan-2-yl]-2-methyl-thiazole 
• 1225301-79-0 2-(5-(4-bromophenyl)furan-2-yl)-2-oxoethyl acetate 
• 1312997-80-0 (S)-1-(5-(4-bromophenyl)furan-2-yl)2-hydroxyethyl acetate 
• 1312997-76-4 (R)-1-(5-(4-bromophenyl)furan-2-yl)ethane-1,2-diyl diacetate 
• 1312997-68-4 2-(5-(4-bromophenyl)furan-2-yl)-2-hydroxyethyl acetate 
• 1312997-64-0 1-(5-(4-bromophenyl)furan-2-yl)2-hydroxyethyl acetate 
• 1312997-60-6 1-(5-(4-bromophenyl)furan-2-yl)ethane-1,2-diyl diacetate 
• 1312997-83-3 (R)-1-(5-(4-bromophenyl)furan-2-yl)ethane-1,2-diol 
• 1225302-11-3 1-(5-(4-bromophenyl)furan-2-yl)ethane-1,2-diol 
• 1225301-95-0 1-(5-(4-bromophenyl)furan-2-yl)-2-hydroxyethanone 
• 42142-99-4 4-[5-(4-bromo-phenyl)-furan-2-yl]-thiazol-2-ylamine 

Relevant academic research and scientific papers

Sequential use of regio- and stereoselective lipases for the efficient kinetic resolution of racemic 1-(5-phenylfuran-2-yl)ethane-1,2-diols

Possible routes for the enzymatic transformation of various substituted 1-(5-phenylfuran-2-yl)ethane-1,2-diols and their mono- and diacetylated counterparts were studied. Combining the regioselectivity of LPS mediated acylation of the starting racemic dio

Substituent effects on the stereochemical outcome of the baker's yeast-mediated biotransformation of α-hydroxy- and α-acetoxymethyl-5-phenylfuran-2-yl-ethanones

In this Letter the baker's yeast-mediated biotransformation of variously substituted α-hydroxy- and α-acetoxymethyl-5-phenylfuran-2-yl-ethanones is described. The stereochemical outcome of the reactions was strongly influenced by the nature of the substituents on the phenyl ring.