Palladium(0)-catalysed regioselective cyclisations of 2-amino(tosyl) benzamides/sulphonamides: the stereoselective synthesis of 3-ylidene-[1,4]benzodiazepin-5-ones/benzo[ f][1,2,5]thiadiazepine-1,1-dioxides

Chem Commun (Camb). 2021 Jun 1;57(44):5462-5465. doi: 10.1039/d1cc00793a.

Abstract

The Pd(0) catalysed cyclisation reactions between tert-butyl propargyl carbonates and 2-aminotosyl benzamides or sulphonamides deliver 1,4-benzodiazepin-5-ones or sultam derivatives, key components of many biologically active compounds. But 2-amino benzamides/sulphonamides require propargyl carbonates substituted at acetylenic carbon to undergo the reaction resulting in the stereoselective formation of the said products.

MeSH terms

  • Benzamides
  • Catalysis
  • Cyclization
  • Molecular Structure
  • Palladium / chemistry*
  • Stereoisomerism
  • Sulfonamides

Substances

  • Benzamides
  • Sulfonamides
  • Palladium