Abstract
The condensation reaction of modified Reissert compounds with aldehydes was investigated. In the reaction of the N-ethoxycarbonyl Reissert analog 1b, ethoxycarbonyl group migration takes place and carbonates of 1-isoquinolylphenylcarbinols (2b, c) are formed. No alkoxycarbonyl group migration was observed in the case of the dihydro-Reissert derivative 6, but the cyclic urethane 7 and the amide 8 were obtained.

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