One-pot multicomponent green Hantzsch synthesis of 1,2-dihydropyridine derivatives with antiproliferative activity

Giovanna Bosica, Kaylie Demanuele, José M. Padrón and Adrián Puerta
Beilstein J. Org. Chem. 2020, 16, 2862–2869. https://doi.org/10.3762/bjoc.16.235

Supporting Information

Supporting Information File 1: Analytical data of the products.
Format: PDF Size: 131.4 KB Download

Cite the Following Article

One-pot multicomponent green Hantzsch synthesis of 1,2-dihydropyridine derivatives with antiproliferative activity
Giovanna Bosica, Kaylie Demanuele, José M. Padrón and Adrián Puerta
Beilstein J. Org. Chem. 2020, 16, 2862–2869. https://doi.org/10.3762/bjoc.16.235

How to Cite

Bosica, G.; Demanuele, K.; Padrón, J. M.; Puerta, A. Beilstein J. Org. Chem. 2020, 16, 2862–2869. doi:10.3762/bjoc.16.235

Download Citation

Citation data can be downloaded as file using the "Download" button or used for copy/paste from the text window below.
Citation data in RIS format can be imported by all major citation management software, including EndNote, ProCite, RefWorks, and Zotero.

Presentation Graphic

Picture with graphical abstract, title and authors for social media postings and presentations.
Format: PNG Size: 8.9 MB Download

Citations to This Article

Up to 20 of the most recent references are displayed here.

Scholarly Works

  • Faizan, M.; Kumar, R.; Mazumder, A.; Salahuddin; Kukreti, N.; Tyagi, P. K.; Kapoor, B. Hantzsch reaction: The important key for pyridine/dihydropyridine synthesis. Synthetic Communications 2024, 54, 1221–1244. doi:10.1080/00397911.2024.2377738
  • Bosica, G.; Abdilla, R. Novel Biopolymer-Based Catalyst for the Multicomponent Synthesis of N-aryl-4-aryl-Substituted Dihydropyridines Derived from Simple and Complex Anilines. Molecules (Basel, Switzerland) 2024, 29, 1884. doi:10.3390/molecules29081884
  • Martinho, L. A.; Andrade, C. K. Z. HPW-Catalyzed environmentally benign approach to imidazo[1,2-a]pyridines. Beilstein journal of organic chemistry 2024, 20, 628–637. doi:10.3762/bjoc.20.55
  • He, Y.; Wang, H.; Ge, C.; Yan, H. A comprehensive discussion on photophysical properties of dihydropyridines: Experimental and theoretical studies. Journal of Molecular Structure 2023, 1281, 135167. doi:10.1016/j.molstruc.2023.135167
  • Peng, H.; Zhang, Y.; Deng, G. Silver(I)-Catalyzed Tandem Reaction of Enynones and 4-Alkenyl Isoxazoles: Synthesis of 2-(Furan-2-yl)-1,2-dihydropyridines. The Journal of organic chemistry 2023, 88, 7038–7045. doi:10.1021/acs.joc.3c00312
  • Maikhuri, V. K.; Verma, V.; Mathur, D.; Prasad, A. K.; Chaudhary, A.; Kumar, R. Sugars in Multicomponent Reactions: A Toolbox for Diversity-Oriented Synthesis. Synthesis 2023, 55, 1007–1041. doi:10.1055/s-0042-1751418
  • Aleksić, J.; Stojanović, M.; Bošković, J.; Baranac-Stojanović, M. Solid-state silica gel-catalyzed synthesis of fluorescent polysubstituted 1,4- and 1,2-dihydropyridines. Organic & biomolecular chemistry 2023, 21, 1187–1205. doi:10.1039/d2ob02119f
  • Vala, R. M.; Patel, H. M. Recent developments in the Hantzsch synthesis of dihydropyridines. Advances in Heterocyclic Chemistry; Elsevier, 2023; pp 179–208. doi:10.1016/bs.aihch.2023.04.001
  • Bosica, G.; Abdilla, R. Recent Advances in Multicomponent Reactions Catalysed under Operationally Heterogeneous Conditions. Catalysts 2022, 12, 725. doi:10.3390/catal12070725
  • Bazani, H. A. G.; Thomé, A.; Affeldt, R. F.; Probst, L. F. D. SBA-15 obtained from rice husk ashes wet-impregnated with metals (Al, Co, Ni) as efficient catalysts for 1,4-dihydropyridine three-component reaction. New Journal of Chemistry 2022, 46, 7899–7909. doi:10.1039/d1nj04835j
  • Sohal, H. S. A review on recent trends in synthesis and applications of 1,4-dihydropyridines. Materials Today: Proceedings 2022, 48, 1163–1170. doi:10.1016/j.matpr.2021.08.209
  • Bosica, G.; Cachia, F.; De Nittis, R.; Mariotti, N. Efficient One-Pot Synthesis of 3,4-Dihydropyrimidin-2(1H)-ones via a Three-Component Biginelli Reaction. Molecules (Basel, Switzerland) 2021, 26, 3753. doi:10.3390/molecules26123753
Other Beilstein-Institut Open Science Activities