110534-46-8

Upstream product

• 64-17-5 ethanol 
• 5720-07-0 4-methoxyphenylboronic acid 

Downstream Products

• 1255509-78-4 (R)-7-chloro-2-(4-methoxyphenyl)-2H-chromene 
• 1255509-81-9 (R)-2-(4-methoxyphenyl)-2H-chromen-7-yl dimethylcarbamate 
• 1255509-72-8 (R)-2-(4-methoxyphenyl)-2H-chromene 
• 41786-36-1 2-(4-methoxyphenyl)-2H-chromene 
• 1334430-54-4 (S)-methyl 2-(((1R,2S)-4-(((benzyloxy)carbonyl)amino)-2-hydroxy-1-(4-methoxyphenyl)butyl)amino)-3-phenylpropanoate 
• 1334430-57-7 benzyl ((3S,4R)-4-(((S)-1,1-dimethoxy-3-phenylpropan-2-yl)amino)-3-hydroxy-4-(4-methoxyphenyl)butyl)carbamate 
• 1334430-50-0 (S)-methyl 2-((1S,2S)-2-hydroxy-1-(4-methoxyphenyl)-3-phenylpropylamino)-3-phenylpropanoate 
• 1334430-49-7 (S)-methyl 2-((1R,2S)-2-hydroxy-1-(4-methoxyphenyl)-3-phenylpropylamino)-3-phenylpropanoate 
• 1334430-52-2 (S)-methyl 2-(((1R,2S)-2-hydroxy-1-(4-methoxyphenyl)-2-phenylethyl)amino)-3-phenylpropanoate 
• 1334430-51-1 (S)-methyl 2-(((1S,2S)-2-hydroxy-1-(4-methoxyphenyl)-2-phenylethyl)amino)-3-phenylpropanoate 
• 1256467-60-3 (1R,2S)-1-(((S)-1,1-dimethoxy-3-phenylpropan-2-yl)amino)-1-(4-methoxyphenyl)-3-phenylpropan-2-ol 
• 1334430-56-6 (1S,2R)-2-(((S)-1,1-dimethoxy-3-phenylpropan-2-yl)amino)-2-(4-methoxyphenyl)-1-phenylethanol 
• 1415559-85-1 (S,E)-6-(1-(4-methoxyphenyl)-3-phenylallyl)benzo[d][1,3]dioxol-5-ol 
• 1415559-84-0 (R,E)-6-(1-(4-methoxyphenyl)-3-phenylallyl)benzo[d][1,3]dioxol-5-ol 

Relevant academic research and scientific papers

Catalytic diastereoselective petasis reactions

Multicomponent Petasis reactions: The first diastereoselective Petasis reaction catalyzed by chiral biphenols that enables the synthesis of syn and anti β-amino alcohols in pure form has been developed. The reaction exploits a multicomponent approach that

Binaphthol-catalyzed asymmetric conjugate arylboration of enones

Conjugate addition of arylboronates to α,β-unsaturated ketones may be catalyzed by chiral binaphthols with enantioselectivities of up to 99:1. Best results were observed with 3,3′-dichloro-BINOL. This chemistry was applied to syntheses of intermediates fo