One-pot enantioselective synthesis of functionalized pyranocoumarins and 2-amino-4H-chromenes: discovery of a type of potent antibacterial agent

J Org Chem. 2012 Jan 20;77(2):878-88. doi: 10.1021/jo202020m. Epub 2012 Jan 4.

Abstract

Function-oriented design and synthesis of chiral small molecules with novel activity is a key goal in modern organic chemistry. As multiple antibiotic-resistant pathogens are emerging and causing serious diseases, the need for practical routes for the development of new types of antibacterial agents is very urgent. Herein, we present a highly efficient process for the synthesis of optically active pyranocoumarins and 2-amino-4H-chromenes through an organocatalytic Knoevenagel/Michael/cyclization sequence, and the preliminary biological studies of these new heterocyclic compounds revealed potent antibacterial activity. This study provides a novel strategy for further research and development of new types of antibacterial agents effective against human pathogens.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amines / chemistry
  • Animals
  • Anti-Bacterial Agents / chemical synthesis
  • Anti-Bacterial Agents / chemistry*
  • Anti-Bacterial Agents / pharmacology*
  • Benzopyrans / chemical synthesis*
  • Chemistry Techniques, Synthetic
  • Cyclization
  • Drug Evaluation, Preclinical / methods
  • Erythrocytes / drug effects
  • Escherichia coli / drug effects
  • HeLa Cells / drug effects
  • Humans
  • Jurkat Cells / drug effects
  • Mice
  • Microbial Sensitivity Tests
  • Molecular Structure
  • Pyranocoumarins / chemical synthesis*
  • Staphylococcus aureus / drug effects
  • Structure-Activity Relationship
  • Toxicity Tests, Chronic

Substances

  • Amines
  • Anti-Bacterial Agents
  • Benzopyrans
  • Pyranocoumarins