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Sn-PILC: A novel Efficient and Recyclable Catalyst for One-pot Three Component Povarov’s Inverse-electron-demand Hetero Diels-Alder Reaction for a Facile Synthesis of Tetrahydropyranoquinoline Derivatives under Neat Conditions
Published
June 30, 2016
Keywords
- Sn-PILC,
- Povarov reaction,
- aza-Diels-Alder,
- THQ,
- neat condition
How to Cite
(1)
Rai, M.; Jadhav, S.; Farooqui, M. Sn-PILC: A Novel Efficient and Recyclable Catalyst for One-Pot Three Component Povarov’s Inverse-Electron-Demand Hetero Diels-Alder Reaction for a Facile Synthesis of Tetrahydropyranoquinoline Derivatives under Neat Conditions. Orbital: Electron. J. Chem. 2016, 8, 149-153.
Copyright (c) 2016 Orbital: The Electronic Journal of Chemistry
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
Abstract
The Povarov’s inverse-electron-demand hetero Diels–Alder one-pot three components reaction of aromatic aldehyde, aromatic amine with DHF has been developed using Sn-PILC as a catalyst under a neat condition which may helpful to society to get pharmacologically more active compounds. In the present study a novel series of tetrahydroquinoline 4(a-f) were synthesized and characterized by IR, 1HNMR, 13CNMR, Mass spectral analysis and elemental analysis. The synthetic details and characterization results are discussed.