1186304-30-2

Upstream product

• 1186304-38-0 C₃₇H₄₀O₈ 
• 621-59-0 isovanillin 
• 1186304-20-0 {4-[5-([1,3]-dioxan-2-yl)-2-methoxyphenoxy]benzyl}triphenylphosphonium bromide 
• 1186304-21-1 2-(2-bromo-5-methoxyphenyl)-1,3-dioxane 
• 1186304-18-6 5-(1,3-dioxan-2-yl)-2-methoxyphenol 
• 1186304-27-7 2-(1,3-dioxan-2-yl)-6-methoxyphenyl trifluoromethanesulfonate 
• 1186304-28-8 2'-(1,3-dioxan-2-yl)-4,6'-dimethoxybiphenyl-2-carbaldehyde 
• 1186304-29-9 C₃₇H₃₈O₈ 
• 1186304-19-7 4-[5-(1,3-dioxan-2-yl)-2-methoxyphenoxy]benzaldehyde 
• 27060-75-9 4-bromo-3-methylanisole 
• 19614-12-1 2-bromo-5-methoxybenzyl bromide 
• 7507-86-0 2-bromo-5-methoxy-benzaldehyde 
• 148-53-8 3-methoxy-2-hydroxybenzaldehyde 
• 1132669-90-9 5-methoxy-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde 

Relevant academic research and scientific papers

Syntheses of macrocyclic bis(bibenzyl) compounds derived from perrottetin e

Macrocyclic bis(bibenzyl) compounds are natural products from liverworts and are of growing interest due to recent reports on new isolated compounds and on their remarkable biological activities. We report here on a flexible and general approach to the to

A synthesis-driven structure revision of 'plagiochin E', a highly bioactive bisbibenzyl

Recently, a bisbibenzyl named plagiochin E showing remarkable antifungal and antitumor activities was isolated from Marchantia polymorpha, a liverwort. The total synthesis of the proposed structure for plagiochin E and of two structurally and biosynthetic