Synthesis of Quinolines from 2-amino aryl ketones: Probing the Lewis Acid Sites of Metal-Organic Framework Catalyst
Author:
Funder
Birla Institute of Technology and Science, Pilani
Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s12039-024-02257-7.pdf
Reference40 articles.
1. Pe E, Samadi A, Carreiras C and Soriano E 2009 Recent Advances in the Friedlander Chem. Rev. 109 2652
2. Akbari J, Heydari A, Kalhor H R and Kohair S A 2010 Sulfonic acid functionalized ionic liquid in combinatorial approach, a recyclable and water tolerant-acidic catalyst for one-pot friedlander quinoline synthesis J. Comb. Chem. 12 137
3. Garella D et al., 2009 Fast, solvent-free, microwave-promoted friedländer annulation with a reusable solid catalyst Synth. Commun. 40 120
4. Martín-Aranda R M and Čejka J 2010 Recent advances in catalysis over mesoporous molecular sieves Top. Catal. 53 141
5. Bose D S and Kumar R K 2006 An efficient, high yielding protocol for the synthesis of functionalized quinolines via the tandem addition/annulation reaction of o-aminoaryl ketones with α-methylene ketones Tetrahedron Lett. 47 813
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