Divergent transformation of C , N -cyclic- N '-acyl azomethine imines by reaction with diazo compounds.

C , N -cyclic- N '-acyl azomethine imines with isoquinoline skeletons were investigated for their reactivity with diazo compounds via two different pathways. During the reaction with ethyl diazoacetate, an α-diazoacetate moiety was introduced at the C1-position of the resulting tetrahydroisoquinolines. Alternatively, diazomethane or trimethylsilyldiazomethane was used to synthesize 3-benzazepine derivatives via ring expansion.