203798-85-0

Basic information

• Product Name: (E)-3-(3,4-Bis-benzyloxy-phenyl)-acrylic acid (R)-2-(3,4-bis-benzyloxy-phenyl)-1-methoxycarbonyl-ethyl ester
• Synonyms: (E)-3-(3,4-Bis-benzyloxy-phenyl)-acrylic acid (R)-2-(3,4-bis-benzyloxy-phenyl)-1-methoxycarbonyl-ethyl ester
• CAS NO: 203798-85-0
• Molecular Weight: 734.846
• Mol File: 203798-85-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (E)-3-(3,4-Bis-benzyloxy-phenyl)-acrylic acid (R)-2-(3,4-bis-benzyloxy-phenyl)-1-methoxycarbonyl-ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-3-(3,4-Bis-benzyloxy-phenyl)-acrylic acid (R)-2-(3,4-bis-benzyloxy-phenyl)-1-methoxycarbonyl-ethyl ester(203798-85-0)
• EPA Substance Registry System: (E)-3-(3,4-Bis-benzyloxy-phenyl)-acrylic acid (R)-2-(3,4-bis-benzyloxy-phenyl)-1-methoxycarbonyl-ethyl ester(203798-85-0)

Safety Data

• Hazardous Substances Data: 203798-85-0(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 99353-00-1 rosmarinic acid methyl ester 
• 203798-70-3 (S)-3-(3,4-Bis-benzyloxy-phenyl)-2-hydroxy-propionic acid methyl ester 
• 203571-41-9 3,4-dibenzyloxycinnamoyl chloride 
• 203798-74-7 (R)-methyl 3-(3,4-bis(benzyloxy)phenyl)-2-hydroxypropanoate 
• 203798-72-5 Benzoic acid (R)-2-(3,4-bis-benzyloxy-phenyl)-1-methoxycarbonyl-ethyl ester 
• 136749-45-6 (+)-(S)-methyl 3-(3,4-dihydroxyphenyl)-2-hydroxypropanoate 
• 100-44-7 benzyl chloride 

Downstream Products

• 1246887-09-1 C₂₃H₂₂O₅ 
• 71038-25-0 methyl (E)-3-(3,4-bis(benzyloxy)phenyl)acrylate 
• 203798-74-7 (R)-methyl 3-(3,4-bis(benzyloxy)phenyl)-2-hydroxypropanoate 
• 99353-00-1 rosmarinic acid methyl ester 

Relevant articles and documents

Explorations of caffeic acid derivatives: Total syntheses of rufescenolide, yunnaneic acids C and D, and studies toward yunnaneic acids A and B

Yunnaneic acids A-D, isolated from the roots of Salvia yunnanensis, are hexameric (A and B) and trimeric (C and D) assemblies of caffeic acid that feature an array of synthetically challenging and structurally interesting domains. In addition to being caffeic acid oligomers, yunnaneic acids A and B are formally dimeric and heterodimeric adducts of yunnaneic acids C and D. Herein we report the first total syntheses of yunnaneic acids C and D featuring the formation of their bicyclo[2.2.2]octene cores in a single step from simple precursors via an oxidative dearomatization/Diels-Alder cascade that may have biogenetic relevance. In addition, exploitation of the key intermediate resulting from this cascade reaction has enabled rapid access to the structurally related caffeic acid metabolite rufescenolide through an unexpected Lewis acid-mediated reduction. Finally, we report the results of extensive model studies toward forming the dimeric yunnaneic acids A and B. These explorations indicate that the innate reactivities of the monomeric fragments do not favor spontaneous formation of the desired dimeric linkages. Consequently, enzymatic involvement may be required for the biosynthesis of these more complex family members.