389634-55-3

Upstream product

• 594-19-4 tert.-butyl lithium 
• 389634-41-7 (4R,5R)-3-[4,5-bis(methoxydiphenyl-methyl)-1,3,2-dioxaborolan-2-yl]furan-2-carbaldehyde 
• 938443-34-6 C₅H₅O₂B(OH)2 
• 389634-39-3 (2R,3R)-1,4-dimethoxy-1,1,4,4-tetraphenyl-2,3-butanediol 2-hydroxymethyl-3-furanylboronate 
• 64817-17-0 3-bromo-2-hydroxymethylfuran 

Downstream Products

• 389634-64-4 (S)-3-(p-toluoyl)-2-(1-hydroxy-2,2-dimethylpropyl)furan 

Relevant academic research and scientific papers

Diastereoselective addition reactions of furyl aldehydes using chiral boronates as auxiliary: Application to the enantioselective synthesis of 2,3-disubstituted furyl alcohols

matrix presented The addition reactions of various nucleophiles to a furyl aldehyde bearing a chiral boronate at the C-3 position furnished chromatographically separable diastereomers. The R diastereoselection was more favorable when no additive was added