186964-34-1

Upstream product

• 186964-32-9 (4,5-Dimethoxy-2-methoxycarbonylmethyl-phenyl)-acetic acid methyl ester 
• 24006-88-0 1,2-Bis(cyanomethyl)-4,5-dimethoxybenzol 
• 186964-33-0 (4,5-Dimethoxy-2-methoxycarbonylmethyl-phenyl)-acetic acid 

Downstream Products

• 186964-38-5 N-[2-(3,4-Dimethoxyphenyl)ethyl]-[2-(2-hydroxyethyl)-4,5-dimethoxyphenyl]acetamid 
• 186964-39-6 [2-(2-Hydroxyethyl)-4,5-dimethoxyphenyl]-N-[2-(3-methoxyphenyl)ethyl]acetamid 

Relevant academic research and scientific papers

Direct benzylic C-H activation for C-O bond formation by photoredox catalysis

Power of light: 1,4-dicyanonaphthalene (DCN) and light directly activates benzylic C-H bonds for intra- and intermolecular C-O bond formation. Arylalkyls have also been transformed directly into aryl ketones using water as a source of oxygen. EDG=electron-donating group, EWG=electron-withdrawing group. Copyright

Synthesis and conformation of hexahydro-isoquino[1,2-b][3]benzazepines

The synthesis of the six hexahydro-isoquino[1,2-b][3]benzazepines 13a-f is described; their conformation is investigated by NMR spectroscopic methods, X-ray analysis and dehydrogenation with mercury(II) acetate. VCH Verlagsgesellschaft mbH, 1997.