Trans-stereoselectivity in the reaction between homophthalic anhydride and imines

Org Lett. 2008 Nov 6;10(21):4759-62. doi: 10.1021/ol801757r. Epub 2008 Sep 25.

Abstract

The reaction between homophthalic anhydride and imines in the presence of TiCl4 and diisopropyl ethyl amine is trans-selective. Under these conditions, the reaction using homochiral imines can be highly diastereoselective, thus allowing the synthesis of enantiopure 1,2,3,4-tetrahydro-1-oxoquinoline-4-carboxylic acids.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Crystallography, X-Ray
  • Imines / chemistry*
  • Models, Molecular
  • Molecular Structure
  • Phthalic Anhydrides / chemistry*
  • Stereoisomerism

Substances

  • Imines
  • Phthalic Anhydrides