130632-09-6

Upstream product

• 104-94-9 4-methoxy-aniline 
• 120-14-9 3,4-dimethoxy-benzaldehyde 

Downstream Products

• 152796-17-3 [(3,4-Dimethoxy-phenyl)-isothiocyanato-methyl]-(4-methoxy-phenyl)-amine 
• 82376-73-6 N-(3,4-dimethoxybenzyl)-4-methoxyaniline 
• 1012886-54-2 methyl 5-(3,4-dimethoxyphenyl)-5-(4-methoxyphenylamino)-4-oxopentanoate 
• 1012886-59-7 methyl 2-(3,4-dimethoxyphenyl)-2-(4-methoxyphenylamino)acetate 
• 1012886-47-3 1-(3,4-dimethoxyphenyl)-1-(4-methoxyphenylamino)propan-2-one 
• 334708-46-2 [2R,3S]-(-)-methyl 3-(3,4-dimethoxyphenyl)-3-(4-methoxyphenylamino)-2-methylpropanoate 

Relevant academic research and scientific papers

Synthesis of novel N-sulfonyl monocyclic β-lactams as potential antibacterial agents

New cis monocyclic β-lactams were synthesized by [2+2] Staudinger cycloaddition reactions of the imine (3,4-dimethoxybenzylidene)-(4- methoxyphenyl)amine and ketenes derived from different acyl chlorides and Et3N. These monocyclic β-lactams wer

Catalytic Asymmetric γ-Lactam Synthesis from Enolisable Anhydrides and Imines

An anion-binding approach to the problem of preparing enantioenriched γ-lactams from enolisable anhydrides and imines is reported. A simple bisurea catalyst promotes the cycloaddition between α-aryl succinic anhydrides and either PMP- or benzhydryl-protec

Application of a catalyst-free Domino Mannich/Friedel-Crafts alkylation reaction for the synthesis of novel tetrahydroquinolines of potential antitumor activity

A useful and efficient method to construct diversely substituted 1,2,3,4-tetrahydroquinolines in good to excellent yields has been developed through a catalyst-free Domino Mannich and intramolecular Friedel-Crafts alkylation reactions of N-arylamines with

Electroreductive acylation of aromatic imines with acylimidazoles

The intermolecular reductive coupling of aromatic imines with acylimidazoles was effected by electroreduction in the presence of chlorotrimethylsilane and gave α-amino-α-aryl ketones. This method was also effective for the synthesis of α-amino-α-aryl esters using methoxycarbonylimidazole as an electrophile.

Transformation of (+)-thiomicamine into a new ligand for the enantioselective addition of methyllithium to prochiral imines

A new ligand 2 was prepared from (+)-thiomicamine 1 and o-methoxyphenol, and its activity as an external controller of stereochemistry in enantioselective additions of methyllithium to prochiral imines 8-10 tested. The non-racemic secondary amines 11-13 w