863498-71-9

Upstream product

• 863498-67-3 methyl{[2'-(3''-phenylprop-1''-ynyl)cyclohept-1'-en-1'-yl]methylene}amine N-oxide 
• 85236-13-1 2-bromocyclohept-1-ene-1-carbaldehyde 
• 863498-63-9 2-(3'-phenylprop-1'-ynyl)cyclohept-1-ene-1-carbaldehyde 

Relevant academic research and scientific papers

The dipolar route to azepin-3-one derivatives by heterocyclization of linear and monocyclic enallenyl nitrones as the key step

The recently discovered transformation of benzopentenynyl nitrones into 1,2-dihydrobenz[c]azepin-3-ones has been extended to the synthesis of structurally different systems including the monocyclic derivatives 17 and 18, the bicyclic azepinones 10a-d, and