155532-86-8

Upstream product

• 50-00-0 formaldehyd 
• 4927-55-3 1,2-bis(3,4-dimethoxyphenyl)ethanone 
• 69151-21-9 1-bromo-1-(3,4-dimethoxyphenyl)ethene 
• 4302-52-7 4-ethynylveratrole 
• 155532-84-6 3-(N,N-dimethylamino)-1,2-bis-(3,4-dimethoxyphenyl)-2-propen-1-one 

Relevant academic research and scientific papers

Approach to phenanthroindolizidine alkaloids using organic azides with 1- Aryl allylic alcohols: Unexpected tandem reactions to indenyl aziridines via nazarov cyclization

Organic azide cyclization reactions with 1- Aryl allylic alcohols were investigated in a synthetic study of phenanthroindolizidine alkaloids. Unsaturated imines (enimines) were effectively obtained from the allylic alcohol adjacent to electron-rich aromat

A convenient alternative route to β-aminoketones

Enaminones has been prepared and submitted to conjugate reduction with LAH and the system Al2O3/R2NH to give β-aminoketones. The latter tandem amination system has also been applied in the Mannich reaction, improving the synthesis of several new diaryl β-aminoketones. Besides, the sequential use of DMFDMA and LAH-CuI on deoxybenzoins furnishes a new route for the synthesis of enones.