Spirobarbiturates with a pyrrolizidine moiety: synthesis, structure and biological evaluation
Abstract
Polycyclic spirobarbiturates containing a pyrrolizidine moiety were synthesized via a one-pot three-component 1,3-dipolar cycloaddition reaction of alloxan, ʟ-proline and N -substituted maleimides. The reaction stereoselectivity was found to depend on the nature of substituents in the maleimide: in most cases the endo -isomer is the main (or only) product, but for some N -arylmaleimides the exo -product is predominant. The proposed mechanism is discussed, and the products were characterized by detailed spectral analysis. The configuration of the stereocenters was determined by X-ray diffraction analysis (XRD) for two adducts, followed by Hirshfeld surface analysis. The antiproliferative effect of the synthesized compounds against cancer cell lines was assessed.
Fields of Study & Subjects
Phosphorus compounds and reactions
Synthesis and Characterization of Pyrroles
Beetle Biology and Toxicology Studies
Publication details
- Journal / source
- Beilstein Journal of Organic Chemistry
- Publisher
- Beilstein Institut
- Volume
- 22
- Pages
- 274–288
- Publication date
- 17 February 2026
- Language
- EN