Catalytic asymmetric allylation of 3,4-dihydroisoquinolines and its application to the synthesis of isoquinoline alkaloids

J Org Chem. 2011 Jan 21;76(2):534-42. doi: 10.1021/jo101956m. Epub 2010 Dec 28.

Abstract

A catalytic asymmetric allylation of 3,4-dihydroisoquinoline was carried out with allyltrimethoxylsilane-Cu as the nucleophile in the presence of DTBM-SEGPHOS as the chiral ligand to afford corresponding chiral 1-allyltetrahydroisoquinoline derivatives in good yield and stereoselectivity. The allyl adduct thus obtained was applied to the synthesis of several isoquinoline alkaloids such as crispine A and homolaudanosine. The reaction was further used for the synthesis of the isoquinoline moiety of schulzeine A.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkaloids / chemical synthesis*
  • Alkaloids / chemistry*
  • Catalysis
  • Copper / chemistry
  • Isoquinolines / chemical synthesis*
  • Isoquinolines / chemistry*
  • Ligands
  • Magnetic Resonance Spectroscopy
  • Molecular Structure
  • Organosilicon Compounds / chemistry
  • Stereoisomerism

Substances

  • Alkaloids
  • G 1616
  • Isoquinolines
  • Ligands
  • Organosilicon Compounds
  • Copper