Die Acetale (I) lassen sich durch die Titelreaktion zu den Isochinolinen (II) (20‐82% Ausbeute) cyclodehydratisieren; unter den Reaktionsbedingungen können dagegen Acetale vom Typ (I) die von in meta‐Stellung unsubstituierten Arylaldehyden oder Ketonen stammen, und das Acetal (I) (R1: ‐H; R2: ‐O‐CH, ‐C6H5) nicht zu Isochinolinen cyclisiert werden.
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