351340-16-4

Upstream product

• 23795-02-0 3-(4-hydroxy-phenyl)-propionic acid ethyl ester 
• 478706-18-2 ethyl 3-{4-[2-benzyloxy-5-(2-ethoxycarbonylethyl)phenoxy]-3-methoxyphenyl}propionate 
• 478706-20-6 3-(4-{2-benzyloxy-5-[2-(methoxymethylcarbamoyl)ethyl]phenoxy}-3-methoxyphenyl)-N-methoxy-N-methylpropionamide 
• 478706-19-3 3-{4-[2-benzyloxy-5-(2-carboxylethyl)phenoxy]-3-methoxyphenyl}propionic acid 
• 478706-17-1 ethyl 3-(4-benzyloxy-3-bromophenyl)propionate 
• 250284-66-3 ethyl 3-(3-bromo-4-hydroxyphenyl)propanoate 
• 704912-95-8 1-(2,4-bis-methoxymethoxy-phenyl)-3-(3-{4-[3-(2,4-bis-methoxymethoxy-phenyl)-3-hydroxy-propyl]-2-methoxy-phenoxy}-4-methoxymethoxy-phenyl)-propan-1-ol 
• 704912-92-5 3-chloro-2-[3-chloro-2-(methoxymethoxy)-5-(3-(tert-butyldimethylsiloxy)propyl)phenoxy]-5-[3-(tert-butyldimethylsiloxy)propyl]phenol 
• 704913-02-0 1-[5-chloro-4-(3-chloro-2-(methoxymethoxy)-5-(3-(tert-butyldimethylsiloxy)propyl)phenoxy)-3-methoxyphenyl]-3-(tert-butyldimethylsiloxy)propane 
• 704913-01-9 C₃₂H₅₁BrCl₂O₅Si₂ 
• 704913-03-1 1-[4-(2-(methoxymethoxy)-5-(3-(tert-butyldimethylsiloxy)propyl)phenoxy)-3-methoxyphenyl]-3-(tert-butyldimethylsiloxy)propane 
• 704912-99-2 acetic acid 3-{4-[5-(3-acetoxy-propyl)-3-chloro-2-methoxymethoxy-phenoxy]-3-bromo-5-chloro-phenyl}-propyl ester 
• 704912-88-9 3-[3-(4-(3-acetyloxypropyl)-2-bromo-6-chlorophenoxy)-5-chloro-1-methoxy-4-oxocyclohexa-2,5-dienyl]propyl acetate 
• 704912-91-4 3-[5-(4-(3-acetyloxypropyl)-2-bromo-6-chlorophenoxy)-3-chloro-4-hydroxyphenyl]propyl acetate 

Relevant academic research and scientific papers

Liebeskind-srogl cross coupling mediated synthesis of verbenachalcone

A flexible and scalable total synthesis of verbenachalcone is achieved in eight linear steps from cheap commercially available starting material, 3-(4-hydroxyphenyl)propanoic acid.

A total synthesis of verbenachalcone, a bioactive diaryl ether from Verbena littoralis

Verbenachalcone 1, isolated from the aerial part of Verbena littoralis H. B. K. (Verbenaceae), has successfully been synthesized by employing anodic oxidation of the phenol derivative 3, as the key step. The bromine and chlorine substituents of 3 effected

Utilization of a copper-catalyzed diaryl ether synthesis for the preparation of verbenachalcone

2-Hydroxy-2′-methoxydiphenyl ethers were efficiently assembled utilizing a catalytic copper mediated coupling of 2-benzyloxybromobenzene derivatives and 2-methoxyphenol derivatives in the presence of cesium carbonate in pyridine followed by debenzylation.