The first example of the Castagnoli-Cushman reaction of homophthalic acid with an amine and an aldehyde conducted in a three-component format is reported. This new protocol employs no dehydrating agents and, unlike the traditional Castagnoli-Cushman reaction of homophthalic anhydride, allows simultaneous mixing of all three reagents and provides good to excellent yields of trans-configured tetrahydroisoquinolonic acids.

Original languageEnglish
Pages (from-to)2595-2599
Number of pages5
JournalTetrahedron Letters
Volume59
Issue number26
DOIs
StatePublished - 27 Jun 2018

    Research areas

  • Azeotropic water removal, Cyclodehydration, Diastereoselectivity, Homophthalic acid, Schiff base, The Castagnoli-Cushman reaction, ONE-POT SYNTHESIS, CATALYST, HOMOPHTHALIC ANHYDRIDE, DICARBOXYLIC-ACIDS, CYCLIC ANHYDRIDES, CONDENSATION, DIVERSITY, CIS-ISOQUINOLONIC ACIDS, INHIBITORS, EFFICIENT

    Scopus subject areas

  • Drug Discovery
  • Biochemistry
  • Organic Chemistry

ID: 34632765