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A NOVEL ROUTE TO THE SYNTHESIS OF SUBSTITUTED N-BENZYL-1,2,3,4-TETRAHYDROISOQUINOLINES. SYNTHESIS OF SENDAVERINE AND CORGOINE
Masood, M.,Tiwari, K. P.
, p. 177 - 182 (2007/10/02)
The condensation product of 2-aminoethanol with substituted benzaldehyde was reduced and N-benzylated with substituted benzyl chloride followed by PPA cyclization to obtain substituted N-benzyl-tetrahydroisoquinolines; likewise the condensation product of
