913648-48-3

Upstream product

• 913648-38-1 2-bromo-5-propoxy-benzoic acid methyl ester 
• 190965-43-6 2-bromo-5-propoxy-benzoic acid 
• 913648-33-6 1-bromo-4-methoxy-2-(2-methoxymethoxyethoxy)benzene 
• 195005-37-9 2-bromo-5-propoxybenzaldehyde 
• 913648-44-9 1-benzo[1,3]-dioxol-5-yl-3-oxo-5-propoxyindane-2-carboxylic acid tert-butyl ester 
• 913648-31-4 toluene-4-sulfonic acid 4-bromo-3-(2-methoxymethoxyethoxy)phenyl ester 
• 913648-40-5 2-(2-tert-butoxycarbonylvinyl)-5-propoxybenzoic acid methyl ester 
• 913648-35-8 4-methoxy-2-(2-methoxymethoxyethoxy)phenylboronic acid 
• 913648-46-1 1-benzo[1,3]-dioxol-5-yl-5-propoxy-3-trifluoromethanesulfonyloxy-1H-indene-2-carboxylic acid tert-butyl ester 
• 494773-45-4 4-bromo-3-hydroxy-phenyl 4-methyl-benzenesulfonate 
• 2973-80-0 2-bromo-5-hydroxybenzaldehyde 
• 6626-15-9 4-Bromoresorcinol 
• 913648-42-7 (-)-(S)-2-(1-benzo[1,3]-dioxol-5-yl-2-tert-butoxy-carbonylethyl)-5-propoxy-benzoic acid methyl ester 

Relevant academic research and scientific papers

1,4-Addition of arylboronic acids to β-aryl-α,β-unsaturated ketones and esters catalyzed by a rhodium(I)-chiraphos complex for catalytic and enantioselective synthesis of selective endothelin A receptor antagonists

An enantioselective synthesis of acyclic β-diaryl ketones and esters via 1,4-addition of arylboronic acids to β-aryl-α,β-unsaturated ketones or esters is described. The complex in situ prepared from [Rh(nbd)2]BF4 and chiraphos was fo