Regioselectivity of Pictet-Spengler cyclization: Synthesis of halotetrahydroisoquinolines

Su Dong Cho, Sang Yong Song, Eun Joo Hur, Ma Chen, Woo Hong Joo, J R Falck, Yong Jin Yoon, Dong Soo Shin

Research output: Contribution to journalArticlepeer-review

16 Scopus citations


The regioselectivity of the Pictet-Spengler cyclization for the synthesis of isoquinolines depends on the aryl substituent at C-2. The ratio of halotetrahydroisoquinoline 4 to isoquinoline 3 increases with increasing electrophilicity of the aromatic ring (H≪I<Br<Cl).

Original languageEnglish (US)
Pages (from-to)6251-6253
Number of pages3
JournalTetrahedron Letters
Issue number36
StatePublished - Sep 3 2001


  • Condensation
  • Cyclization
  • Halotetrahydroisoquinoline
  • Pictet-Spengler

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry


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