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Abstract
Lithium aluminum hydride reduced enamines of the 3,3-dialkyl-3,4-dihydroisoquinoline series to the corresponding tetrahydroisoquinolines. In the presence of a hydrogen atom at the Β-carbon atom of the enamino ester the action of lithium aluminum hydride and alkylmagnesium bromide leads to the products from the condensation of two molecules of the initial compound.
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