NMR spectroscopic and computational analysis of E / Z isomerism in imines derived from isatin
Abstract
ratio in solution is shown to depend strongly on stabilization by solvent interactions and substituents attached to the imine nitrogen. Predominant isomer structures are typically stabilized by π-stacking between aromatic rings, highlighting the key role of non-covalent interactions in determining stereochemical products.
Fields of Study & Subjects
Organic Chemistry Cycloaddition Reactions
Asymmetric Synthesis and Catalysis
Structural and Chemical Analysis of Organic and Inorganic Compounds
Publication details
- Journal / source
- RSC Advances
- Publisher
- Royal Society of Chemistry (RSC)
- Volume
- 16
- Issue
- 14
- Pages
- 12238–12245
- Publication date
- 1 January 2026
- Language
- EN