Abstract
AbstractPhenolic cyclization of 3‐hydroxy phenethylamine with acylbutyric acid and acylpropionic acid afforded the lactam of the corresponding benzol[a] quinolizine and pyrrolo[2, 1‐a]isoquinoline derivatives, which were reduced with lithium aluminum hydride to give the benzol[a]quinolizine and pyrrolo[2,1 ‐a] isoquinoline derivatives, respectively. The configurations of acetyl derivatives of these products were determined.
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