67707-65-7

Upstream product

• 303024-56-8 N-(4-nitrobenzyl)-4-methylbenzamide 
• 874-60-2 4-methyl-benzoyl chloride 
• 18600-42-5 4-nitrobenzylamine hydrochloride 

Downstream Products

• 67707-66-8 C₁₅H₁₂N₂O₂ 
• 212253-99-1 p-Methyl-N-(p-nitrobenzyl)benzimidoyl isothiocyanate 
• 212254-00-7 1-Methyl-3-{[(E)-4-nitro-benzylimino]-p-tolyl-methyl}-1-phenyl-thiourea 
• 128694-32-6 5-Ethylsulfanyl-6,6,7,7-tetramethyl-4-(4-nitro-phenyl)-2-p-tolyl-1,3-diaza-bicyclo[3.2.0]hept-2-ene 
• 128694-28-0 5-Ethoxy-6,6,7,7-tetramethyl-4-(4-nitro-phenyl)-2-p-tolyl-1,3-diaza-bicyclo[3.2.0]hept-2-ene 

Relevant academic research and scientific papers

Reaction of nitrile ylides with isatins and o-benzoquinones: Formation of novel spirooxazoline derivatives

Nitrile ylide generated by the base catalysed reaction of imidoyl chlorides underwent dipolar cycloaddition with isatins, phenanthrenequinone and acenaphthenequinone to afford novel spirooxazoline derivatives.

1,3-Dipolar Cycloadditions of 2-Ethoxy- and 2-(Ethylthio)-1-azetines with Nitrile Oxides, Nitrile Ylides and Nitrilimines: An Unexpected 1,2,4-Triazole Formation.

2-Ethoxy- and 2-(ethylthio)-1-azetines readily undergo 1,3-dipolar cycloadditions with nitrile oxides and nitrile ylides to give stable 4,5-bicyclic cycloadducts.With nitrilimines, however, the expected 1,3-dipolar cycloadducts and/or unexpected ring-open