Affiliation:
1. Department of Chemistry, Faculty of Physics & Chemistry, Alzahra University, Tehran, Iran
Abstract
In this review, we try to highlight the significance, mechanism propositions, computational and experimental assessments of Hantzsch dihydropyridine (DHPs) which readily oxidized to the corresponding pyridines as one of the most important aromatic heterocycles. We also try to give an overview to its ability in transfer hydrogenation, acting as hydride donors from computational and experimental points of view. Our survey is also extended to computational assessments on the structural and biological properties of Hantzsch DHPs.
Publisher
Bentham Science Publishers Ltd.
Reference149 articles.
1. Hantzsch A.; Ueber die synthese pyridinartiger verbindungenaus acetessigäther und aldehyd ammoniak. Justus Liebigs Ann Chem 1882,215,1-82
2. Wan J.P.; Liu Y.; Recent advances in new multicomponent synthesis of structurally diversi-fied 1,4-dihydropyridines. RSC Advances 2012,2,9763-9777
3. Heravi M.M.; Behbahani F.K.; Oskooie H.A.; Shoar R.H.; Catalytic aromatization of Hantzsch 1, 4-dihydropyridines by ferric perchlorate in acetic acid. Tetrahedron Lett 2005,46,2775-2777
4. Xia J.J.; Wang G.W.; One-Pot Synthesis and aromatization of 1,4-dihydropyridines in refluxing water. Chem Commun (Camb) 2005,14,2379-2383
5. Katritzky A.R.; Ostercamp D.L.; Yousaf T.I.; The mechanisms of heterocyclic ring closures. Tetrahedron 1987,43,5171-5186
Cited by
4 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献