Novel chiral C1-1′,2′,3′,4′-tetrahydro-1,1′- bisisoquinolines: synthesis, resolution, and applications in catalytic enantioselective reactions

Gao Qi, Yao Qiong Ji, Zaher M.A. Judeh*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

23 Citations (Scopus)

Abstract

A straightforward synthesis of a structurally constrained C1-1′,2′,3′,4′-tetrahydro-1,1′- bisisoquinoline 1 is described. Resolution of this compound has been achieved successfully. The preparation of chiral N-alkyl, urea, and thiourea derivatives as potential new chiral ligands, based on the parent compound 1, is reported. Chiral compound 1 induced very good selectivity and yield in the addition of either Et2Zn (85% ee, 96% yield) or nitromethane (85% ee, 60% yield) to benzaldehyde.

Original languageEnglish
Pages (from-to)4195-4205
Number of pages11
JournalTetrahedron
Volume66
Issue number23
DOIs
Publication statusPublished - Jun 5 2010
Externally publishedYes

ASJC Scopus Subject Areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

Keywords

  • Bischler-Napieralski reaction
  • Bisisoquinolines
  • C-C bond forming reactions
  • Henry reaction

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