350792-41-5

Upstream product

• 52702-30-4 2<(methoxymethyl)oxy>phenol 
• 120-80-9 benzene-1,2-diol 

Downstream Products

• 88275-88-1 3-bromo-2-methoxyphenol 
• 1613299-26-5 3-bromo-5-(1H-indol-3-yl)-2-methoxyphenol 
• 1613299-27-6 5-[5-(benzyloxy)-1H-indol-3-yl]-3-bromo-2-methoxyphenol 
• 1613299-38-9 3-bromo-5-(1-ethyl-1H-indol-3-yl)-2-methoxyphenol 
• 1613299-42-5 3-bromo-2-methoxy-5-(2-methyl-1H-indol-3-yl)phenol 
• 944334-08-1 2-cyclopropylmethoxy-1-iodo-3-methoxymethoxybenzene 
• 944334-12-7 3-bromo-6-difluoromethoxy-2-iodophenol 
• 944334-09-2 2-cyclopropylmethoxy-3-iodophenol 

Relevant academic research and scientific papers

Access to 3-arylindoles through a tandem one-pot protocol involving dearomatization, a regioselective michael addition reaction, and rearomatization

A facile, general and rapid protocol for the introduction of oxygenated aryls at the 3-position of indoles is described. This approach consists of a tandem dearomatization, a regioselective Michael addition reaction, and rearomatization in a one-pot three-step sequence to obtain 3-arylindoles in good yields. A non-metal mediated detour method for installing oxygenated aryls at the 3-position of indoles is described. Copyright

An efficient preparation of 6-alkoxy-substituted benzocyclobutenones

A short, efficient route to 3-alkoxybenzynes has been developed, starting from readily available compounds. This has enabled rapid access to 6-alkoxybenzocyclobutenones, which are valuable synthetic intermediates.