
Scientific Reports, Journal Year: 2024, Volume and Issue: 14(1)
Published: Nov. 30, 2024
Aza-Diels–Alder cycloaddition reaction is a critical synthetic method for the production of bioactive tetrahydroquinolines. To this aim, an imine obtained from aniline derivative and carbonyl compound cyclized with alkene in presence catalyst. In research, some tetrahydroquinoline compounds are synthesized through aza-Diels–Alder prepared Ce(III) immobilized on functionalized halloysite (Ce/Hal-TCT-IDA) as Ce/Hal-TCT-IDA was by incorporation aminopropyl silane surface, followed treatment 2,4,6-trichloro-1,3,5-triazine (TCT) iminodiacetic acid (IDA), loading cerium nitrate. Then, it characterized analyzed different analytical methods, indicating amorphous agglomerated grains (20–60 nm), containing 0.00196 mmol g−1 ions. The catalytic activity reusability were studied research.
Language: Английский