CiteScore: 1.9     h-index: 21

Document Type : Original Research Article

Authors

Department of Chemistry, Payame Noor University, PO Box 19395-3697, Tehran, Iran

Abstract

Dihydropyridine derivatives have been identified as calcium channel blockers and are predominantly utilized in cosmetics and pharmaceuticals. These compounds are often used as intermediates for producing biologically active products, including drugs, herbicides, insecticides, and fungicides. The applications of pyridines and their benzo derivatives have been described over the past decade along with natural products containing the pyridine ring system. These applications are classified into three categories: biological, chemical and functional. Functional applications based on the physical properties of pyridines and their benzo-derived compounds describe colors, flavors, and ionic liquids. Chemical applications, based on the chemical properties of pyridines and benzo derivatives, describe reagents in analytical chemistry as well as catalysts and reagents in organic synthesis. Biological applications based on the environmental activity of pyridine compounds in pharmaceutical, agrochemical and veterinary products have been presented in this study. In this research study, the synthesis of 1,4-Dihydropyridine derivatives was investigated through a three-component one-pot reaction using nano-cerium oxide catalyst.

Graphical Abstract

One-pot synthesis of 1,4-dihydropyridine derivatives using nano-cerium oxide as an efficient catalyst

Keywords

Main Subjects

[1]. Altaf A.A., Shahzad A., Gul Z.J. Drug. Design. Med. Chem., 2015, 1:1
[2]. Schmidt Bi.E., Haderlein T.C. Environment. Sci. Technol. 2006, 19:5962
[3]. O’Loughlin E.J., Traina S.J., Sims G.K. Environment. Toxicol. Chem., 2000, 19:2168
[4]. Baran Das A., Chandon D. Science. Beverages., 2019, 14:539
[5]. Bor T., Aljaloud S.O., Gyawali R., Ibrahim S.A. Fruits. Vegetables. Herbs., 2016, 26:551
[6]. Mahinpour R., Moradi L., Zahraei Z., Pahlevanzadeh N. J. Saud. Chem. Soc., 2018, 22:876
[7]. Mathur R., Negi Kh.S., Shrivastava R., Nair R. RSC Adv., 2021, 11:1376
[8]. Teimouri A., Ghorbanian L., Moatari A. Bull. Chem. Soc. Ethiop., 2013, 27:427
[9]. Maleki A., Kamalzare M., Aghaei M. J. Nanostruct. Chem., 2015, 5:95
[10]. Colon G., Navio J.A.,  Monaci R., Ferino I. Physical. Chem. Physics., 2000, 19:84
[11]. Shahidi F., Senadheera R. Encyclopedia of food chemistry., 2010, 50:497
[12]. Song Z., Chaochao D., Shaoli W., Qian D., Yaoguang S., Zhilong Z., Guang L. Chem. Commun., 2020, 12:1
[13]. Swarnalatha G., Prasanthi G., Sirisha N., Madhusudhana Chetty, C. International. J. Chem. Tech. Research., 2011, 3:75
[14]. Zhao S., Gorte R.A. Appl. Catal. 2004, 277:129
[15]. Taghavi Fardood S., Ramazani A., Joo S.W. J. Appl. Chem. Res., 2017, 11:8
[16]. Al Banna L.S., Salem N.M., Jaleel G.A., Awwad A.M. Chem. Int., 2020, 6:137
[17]. Matin T.A.B., Ghasemi N., Ghodrati K., Ramezani M. Eur. Chem. Commun., 2019, 1:494
[18]. Taghavi Fardood S., Moradnia F., Moradi S., Forootan R., Yekke Zare F., Heidari M. Nanochem. Res., 2019, 4:140
[19]. Taghavi Fardood S., Moradnia F., Ramezani A. Micro. Nano. Lett., 2019, 14:986
[20]. Taghavi Fardood S., Moradnia F., Mostafaei M., Afshari Z., Faramarzi V., Ganjkhanlu S. Nanochem. Res., 2019, 4:86
[21]. Moradnia F., Taghavi Fardood S., Ramazani A., Gupta V.K. J. Photochem. Photobiol. A: Chem., 2020, 392:112433
[22]. Taghavi Fardood S., Forootan R., Moradnia F., Afshari Z., Ramazani A. Material. Res. Express., 2020, 7:015086
[23]. Taghavi Fardood S., Ramazani A., Moradnia F., Afshari Z., Ganjkhanlu S., Yekke Zare F. Chem. Method., 2019, 3:696
[24]. Moradnia F., Ramazani A., Taghavi Fardood S., Gouranlou F. Material. Research. Express., 2019, 6:075057
[25]. Ramazani A., Farshadi A., Mahyari A., Sadri F., Joo S.W. Azimzadeh Asiabi P., Taghavi Fardood S., Dayyani N., Ahankar H. Int. J. Nano Dimens., 2016, 7:41
[26]. Taghavi Fardood S., Ramazani A., Ayubi M., Moradnia F., Abdpour Sh., Forootan R. Chemical Methodologies, 2019, 3:519
[27]. Ramazani A., Mahyari A. Helv. Chim. Acta, 2010, 93:2203
[28]. Ezzatzadeh E., Zamani Hargalani F., Shafaei F. Polycyclic. Aromatic. Compounds, 2021. https://doi.org/10.1080/10406638.2021.1879882
[29]. Sadeghi Meresht A., Ezzatzadeh E., Dehbandi B., Salimifard M., Rostamian R. Polycyclic. Aromatic. Compounds., 2021. doi.org/10.1080/10406638.2021.1913426 online
[30]. Ezzatzadeh E., Hossaini Z. Appl. Organomet. Chem., 2020, 34:e5596
[31]. Ezzatzadeh E., Hossaini Z. Mol. Diver., 2019, 24:81
[32]. Ezzatzadeh E. Zeitschrift. Für. Naturforschung., 2018, 73:179
[33]. Davoodnia A., Bakavoli M., Moloudi R., Tavakoli-Hoseini N., Khashi M. Monatsh. Chemist., 2010, 141:867
[34]. Lin K.S., Chowdhury S. International. J. Mol. Science., 2010, 1:3226
[35]. Sheik Mansoor S., Aswin K., Logaiya K., Sudhan S.P.N. J. King Saud. Univers. Science., 2013, 25:191