208399-65-9

Upstream product

• 208399-63-7 4-(5-[1,3]Dioxolan-2-yl-2-methoxy-phenoxy)-benzoic acid methyl ester 
• 109694-35-1 4-(5-diacetoxymethyl-2-methoxy-phenoxy)-3-nitro-benzoic acid methyl ester 
• 101274-71-9 4-(5-formyl-2-methoxy-phenoxy)-3-nitro-benzoic acid methyl ester 
• 101110-74-1 methyl 4-(5'-formyl-2'-methoxyphenoxy)benzoate 
• 14719-83-6 methyl 3-nitro-4-chlorobenzoate 
• 621-59-0 isovanillin 
• 181758-85-0 2-(3-hydroxy-4-methoxyphenyl)-1,3-dioxolane 
• 459-57-4 4-fluorobenzaldehyde 
• 208399-64-8 {4-[5-(1,3-dioxolan-2-yl)-2-methoxyphenoxy]phenyl}methanol 

Downstream Products

• 208399-69-3 methyl 4-{2-[2-{4-[5-(1,3-dioxolan-2-yl)-2-methoxyphenoxy]phenyl}-1-ethenyl]-4-methoxyphenyl}-3-methoxybenzoate 
• 1034145-79-3 methyl 4-{2-[2-{4-[5-(1,3-dioxolan-2-yl)-2-methoxyphenoxy]phenyl}-1-ethenyl]phenyl}benzoate 
• 1034145-77-1 methyl 4-{2-[2-{4-[5-(1,3-dioxolan-2-yl)-2-methoxyphenoxy]phenyl}-1-ethenyl]-4-methoxyphenyl}benzoate 
• 1034145-76-0 methyl 4-{2-[2-{4-[5-(1,3-dioxolan-2-yl)-2-methoxyphenoxy]phenyl}-1-ethenyl]phenyl}-3-methoxybenzoate 
• 208399-70-6 methyl 4-(2-{4-[5-(1,3-dioxolan-2-yl)-2-methoxyphenoxy]phenethyl}-4-methoxyphenyl)-3-methoxybenzoate 
• 208399-71-7 [4-(2-{4-[5-(1,3-dioxolan-2-yl)-2-methoxyphenoxy]phenethyl}-4-methoxyphenyl)-3-methoxyphenyl]methanol 
• 208399-64-8 {4-[5-(1,3-dioxolan-2-yl)-2-methoxyphenoxy]phenyl}methanol 
• 111436-61-4 3-[4-(bromomethyl)phenoxy]-4-methoxybenzaldehyde 

Relevant academic research and scientific papers

Co-existence of α-glucosidase-inhibitory and liver X receptor-regulatory activities and their separation by structural development

Liver X receptors (LXR), which were originally reported as oxysterol-activated nuclear receptors, were recently found to recognize glucose as a physiological ligand. On this basis, we have already developed novel LXR antagonists based upon α-glucosidase i

Total synthesis of cavicularin and riccardin C: Addressing the synthesis of an arene that adopts a boat configuration

(Chemical Equation Presented) A transannular ring contraction induced by the addition of an aryl radical intermediate to a proximal arene facilitated the construction of the highly strained macrocyclic core of cavicularin (1). The precursor, an iodinated

Syntheses of Cyclic Bisbibenzyl Systems

The cyclic bisbibenzyl systems Marchantin I (3), Riccardin C (4) and Isoplagiochin C (5) representing unique types of bryophyte constituents were prepared by a flexible, efficient and general synthetic approach involving the construction of biphenyl and bibenzyl units using Suzuki and Wittig protocols.