30223-86-0

Upstream product

• 21615-75-8 3-(4-tolyl)-isobenzofuranone 
• 1401613-80-6 C₃₅H₃₈O₄ 

Downstream Products

• 802613-56-5 N-Ethyl-4-benzanthracen-7-yl-N-(2-hydroxyethyl)-benzylamin 
• 801209-58-5 N-Ethyl-4-benzanthracen-7-yl-N-(2-chlorethyl)-benzylamin 
• 802325-27-5 4-Benzanthracen-7-yl-N-(3-hydroxypropyl)-benzylamin 
• 701190-68-3 4-Benzanthracen-7-yl-N-(2-hydroxyethyl)-N-methyl-benzylamin 
• 802044-09-3 4-Benzanthracen-7-yl-N-(3-chlorpropyl)-benzylamin 
• 739306-88-8 4-Benzanthracen-7-yl-N-(2-chlor-ethyl)-N-methyl-benzylamin 
• 30223-87-1 7-<4-Brommethyl-phenyl>-benzanthracen, 4-Benzanthracen-7-yl-benzylbromid 

Relevant academic research and scientific papers

Synthesis of annulated arenes and heteroarenes involving lewis acid-mediated regioselective annulation of unsymmetrical 1,2-(Diaryl/ diheteroarylmethine)dipivalates

A ZnBr2-mediated regioselective annulation of unsymmetrical 1,2-diarylmethinedipivalates in DCM at room temperature led to the formation of annulated arenes and heteroarenes. The annulation of the dipivalate proceeds through the intermediacy of