236751-58-9

Upstream product

• 236751-54-5 3-chloro-2,5-dimethoxybenzyl alcohol 
• 18113-03-6 2-chloro-4-methoxyphenol 
• 1007853-31-7 2-chloro-6-(hydroxymethyl)-4-methoxyphenol 

Downstream Products

• 236751-71-6 7-chloro-4-hydroxy-5,8-dimethoxy-2-naphthoic acid 
• 152039-03-7 ethyl 4-acetoxy-7-chloro-5,8-dimethoxy-2-naphthoate 
• 236751-86-3 methyl (+/-)-3-(6-chloro-1-hydroxy-3-hydroxymethyl-5,8-dimethoxynaphthalen-2-yl)-2-hydroxy-4-hydroxymethyl-6-methylbenzoate 
• 236751-82-9 methyl (+/-)-3-(6-chloro-1-hydroxy-3-hydroxymethyl-5,8-dimethoxynaphthalen-2-yl)-2-hydroxy-4-(methoxymethoxy)methyl-6-methylbenzoate 
• 236751-74-9 2-iodo-6-methoxycarbonyl-3-(methoxymethoxy)methyl-5-methylphenyl 7-chloro-4-hydroxy-5,8-dimethoxy-2-naphthoate 
• 1369490-82-3 2-chloro-6-(1,3-dioxan-2-yl)cyclohexa-2,5-diene-1,4-dione 
• 1369490-75-4 2-(3-chloro-2,5-dimethoxyphenyl)-1,3-dioxane 

Relevant academic research and scientific papers

General synthesis route to benanomicin-pradimicin antibiotics

A general approach to the regio- and stereoselective total synthesis of the benanomicin-pradimicin antibiotics (BpAs) is described. Construction of the aglycon has been achieved by 1)the diastereoselective ring-opening of a biaryl lactone by using (R)-val