References
- Neochoritis, C. G.; Zhao, T.; Dömling, A. Tetrazoles via Multicomponent Reactions. Chem. Rev. 2019, 119, 1970–2042. DOI: 10.1021/acs.chemrev.8b00564.
- Abyar, S.; Khandar, A. A.; Salehi, R.; Abolfazl Hosseini-Yazdi, S.; Alizadeh, E.; Mahkam, M.; Jamalpoor, A.; White, J. M.; Shojaei, M.; Aizpurua-Olaizola, O.; et al. In Vitro Nephrotoxicity and Anticancer Potency of Newly Synthesized Cadmium Complexes. Sci. Rep. 2019, 9, 14686. DOI: 10.1038/s41598-019-51109-9.
- Zeisel, L.; Szimhardt, N.; Wurzenberger, M. H. H.; Klapötke, T. M.; Stierstorfer, J. 2-Methyl-Substituted Monotetrazoles in Copper(Ii) Perchlorate Complexes: Manipulating Coordination Chemistry and Derived Energetic Properties. New J. Chem. 2019, 43, 609–616. DOI: 10.1039/C8NJ05375H.
- Li, Y.; Zhang, X.; Lan, J.; Xu, P.; Sun, J. Porous Zn(Bmic)(at) MOF with Abundant Amino Groups and Open Metal Sites for Efficient Capture and Transformation of CO2. Inorg. Chem. 2019, 58, 13917–13926. DOI: 10.1021/acs.inorgchem.9b01762.
- Gu, X. Q.; Wu, T. Y.; Su, W. T.; Shi, Y. J.; Wang, Z. K.; Li, Y.; Liu, X. Y.; Li, Q. Y.; Yang, G. W. Synthesis, Crystal Structure and Luminescence of Two Barium(II) Compounds: From Mono- to Bis-Tetrazole Carboxylic Acids. J. Iran. Chem. Soc. 2019, 16, 449–454. DOI: 10.1007/s13738-018-1515-8.
- Zhang, G.; Li, G.; Heil, T.; Zafeiratos, S.; Lai, F.; Savateev, A.; Antonietti, M.; Wang, X. Tailoring the Grain Boundary Chemistry of Polymeric Carbon Nitride for Enhanced Solar Hydrogen Production and CO2 Reduction. Angew. Chem. Int. Ed. Engl. 2019, 58, 3433–3437. DOI: 10.1002/anie.201811938.
- Nasrollahzadeh, M.; Sajjadi, M.; Khonakdar, H. A. Synthesis and Characterization of Novel Cu(II) Complex Coated Fe3O4@SiO2 Nanoparticles for Catalytic Performance. J. Mol. Struct. 2018, 1161, 453–463. DOI: 10.1016/j.molstruc.2018.02.026.
- Hassankhani, A.; Gholipour, B.; Rostamnia, S. An Efficient Regioselective Three-Component Synthesis of Tetrazoloquinazolines Using g-C3N4 Covalently Bonded Sulfamic Acid. Polyhedron. 2020, 175, 114217. DOI: 10.1016/j.poly.2019.114217.
- Firoj Basha, S.; Prasad, T. N.; Gudise, V. B.; Kumar, V. S.; Mulakayala, N.; Anwar, S. An Efficient, Multicomponent, Green Protocol to Access 4, 7-Dihydrotetrazolo [1, 5-a] Pyrimidines and 5,6,7,9-Tetrahydrotetrazolo[5,1-b]Quinazolin-8(4H)-Ones Using PEG-400 under Microwave Irradiation. Synth. Commun. 2019, 49, 3181–3190. DOI: 10.1080/00397911.2019.1659973.
- Scheuermann, T. H.; Stroud, D.; Sleet, C. E.; Bayeh, L.; Shokri, C.; Wang, H.; Caldwell, C. G.; Longgood, J.; MacMillan, J. B.; Bruick, R. K.; et al. Isoform-Selective and Stereoselective Inhibition of Hypoxia Inducible Factor-2. J. Med. Chem. 2015, 58, 5930–5941. DOI: 10.1021/acs.jmedchem.5b00529.
- Pallandre, J.-R.; Borg, C.; Rognan, D.; Boibessot, T.; Luzet, V.; Yesylevskyy, S.; Ramseyer, C.; Pudlo, M. Novel Aminotetrazole Derivatives as Selective STAT3 Non-Peptide Inhibitors. Eur. J. Med. Chem. 2015, 103, 163–174. DOI: 10.1016/j.ejmech.2015.08.054.
- Nimnual, P.; Tummatorn, J.; Boekfa, B.; Thongsornkleeb, C.; Ruchirawat, S.; Piyachat, P.; Punjajom, K. Construction of 5-Aminotetrazoles via in Situ Generation of Carbodiimidium Ions from Ketones Promoted by TMSN3/TfOH. J. Org. Chem. 2019, 84, 5603–5613. DOI: 10.1021/acs.joc.9b00555.
- Bhagat, S. B.; Telvekar, V. N. L. Proline: An Efficient Organocatalyst for the Synthesis of 5-Substituted 1H-Tetrazoles via [3 + 2] Cycloaddition of Nitriles and Sodium Azide. Synlett. 2018, 29, 874–879. DOI: 10.1055/s-0036-1591534.
- Garbrecht, W. L.; Herbst, R. M. The Synthesis of Certain 5-Aminotetrazole Derivatives. I. The Action of Hydrazoic Acid on Some Dialkylcyanamides. J. Org. Chem. 1953, 18, 1003–1013. DOI: 10.1021/jo50014a015.
- Habibi, D.; Nasrollahzadeh, M.; Sahebekhtiari, H.; Sajadi, S. M. Ultrasound-Promoted Regioselective Synthesis of 1-Aryl-5-Amino-1H-Tetra-Zoles. Synlett. 2012, 23, 2795–2798. DOI: 10.1055/s-0032-1317513.
- Khalili, B.; Darabi, F. S.; Eftekhari-Sis, B.; Rimaz, M. Green Chemistry: ZrOCl2·8H2O Catalyzed Regioselective Synthesis of 5-Amino-1-Aryl-1H-Tetrazoles from Secondary Arylcyanamides in Water. Monatsh. Chem. 2013, 144, 1569–1572. DOI: 10.1007/s00706-013-1038-z.
- Habibi, D.; Nasrollahzadeh, M.; Faraji, A. R.; Bayat, Y. Efficient Synthesis of Arylaminotetrazoles in Water. Tetrahedron. 2010, 66, 3866–3870. DOI: 10.1016/j.tet.2010.03.003.
- Sajjadi, M.; Nasrollahzadeh, M.; Mohammad Sajadi, S. Green Synthesis of Ag/Fe(3)O(4) nanocomposite using Euphorbia peplus Linn leaf extract and evaluation of its catalytic activity. J. Colloid Interface Sci. 2017, 497, 1–13. DOI: 10.1016/j.jcis.2017.02.037.
- Motahharifar, N.; Nasrollahzadeh, M.; Taheri-Kafrani, A.; Varma, R. S.; Shokouhimehr, M. Magnetic Chitosan-Copper Nanocomposite: A Plant Assembled Catalyst for the Synthesis of Amino- and N-Sulfonyl Tetrazoles in Eco-Friendly Media. Carbohydr. Polym. 2020, 232, 115819. DOI: 10.1016/j.carbpol.2019.115819.
- Nasrollahzadeh, M.; Habibi, D.; Shahkarami, Z.; Bayat, Y. A General Synthetic Method for the Formation of Arylaminotetrazoles Using Natural Natrolite Zeolite as a New and Reusable Heterogeneous Catalyst. Tetrahedron. 2009, 65, 10715–10719. DOI: 10.1016/j.tet.2009.10.029.
- Habibi, D.; Nasrollahzadeh, M.; Bayat, Y. AlCl3 as an Effective Lewis Acid for the Synthesis of Arylaminotetrazoles. Synth. Commun. 2011, 41, 2135–2145. DOI: 10.1080/00397911.2010.497728.
- Habibi, D.; Nasrollahzadeh, M. Synthesis of Arylaminotetrazoles by ZnCl2/AlCl3/Silica as an Efficient Heterogeneous Catalyst. Monatsh. Chem. 2012, 143, 925–930. DOI: 10.1007/s00706-011-0670-8.
- Habibi, D.; Nasrollahzadeh, M. ZnO as an Effective and Reusable Heterogeneous Catalyst for the Synthesis of Arylaminotetrazoles. Synth. Commun. 2012, 42, 2023–2032. DOI: 10.1080/00397911.2010.548620.
- Bahari, S.; Sabegh, M. A. Nano Indium Oxide as a Recyclable Catalyst for the Synthesis of Arylaminotetrazoles. J. Chem. Sci. 2013, 125, 153–157. DOI: 10.1007/s12039-012-0348-8.
- Bahari, S.; Rezaei, A. CoFe2O4 Nanoparticles as a Magnetically Recoverable and Reusable Catalyst for the Synthesis of Arylaminotetrazoles and 5-Aryloxytetrazoles. J. Chem. Res. 2014, 38, 65–68. DOI: 10.3184/174751914X13871210981307.
- Habibi, D.; Faraji, A. R.; Sheikh, D.; Sheikhi, M.; Abedi, S. Application of Supported Mn(Iii), Fe(Iii) and Co(Ii) as Heterogeneous, Selective and Highly Reusable Nano Catalysts for Synthesis of Arylaminotetrazoles, and DFT Studies of the Products. RSC Adv. 2014, 4, 47625–47636. DOI: 10.1039/C4RA06463A.
- Maham, M.; Khalaj, M. Synthesis of Thiotetrazoles and Arylaminotetrazoles Using Rutile Tio2 Nanoparticles as a Heterogeneous and Reusable Catalyst. J. Chem. Res. 2014, 38, 502–506. DOI: 10.3184/174751914X14061217395813.
- Habibi, D.; Heydari, S.; Afsharfarnia, M.; Rostami, Z. A Versatile Synthesis of Arylaminotetrazoles by a Magnetic Fe@Phendiol@Mn Nano-Particle Catalyst and Its Theoretical Studies. Appl. Organometal. Chem. 2017, 31, e3826. DOI: 10.1002/aoc.3826.
- Modarresi-Alam, A. L. I. R.; Nasrollahzadeh, M. Synthesis of 5-Arylamino-1H (2H)-Tetrazoles and 5-Amino-1-Aryl-1H-Tetrazoles from Secondary Arylcyanamides in Glacial Acetic Acid: A Simple and Efficient Method. Turkish J. Chem. 2009, 33, 267–280.
- Habibi, D.; Nasrollahzadeh, M. Silica-Supported Ferric Chloride (FeCl3-SiO2): an Efficient and Recyclable Heterogeneous Catalyst for the Preparation of Arylaminotetrazoles. Synth. Commun. 2010, 40, 3159–3167. DOI: 10.1080/00397910903370683.
- Khamooshi, F.; Modarresi-Alam, A. R. Solvent-Free Preparation of Arylaminotetrazole Derivatives Using Aluminum(III) Hydrogensulfate as an Effective Catalyst. Chinese Chem. Lett. 2010, 21, 892–896. DOI: 10.1016/j.cclet.2010.03.008.
- Taheri-Ledari, R.; Rahimi, J.; Maleki, A. Synergistic Catalytic Effect between Ultrasound Waves and Pyrimidine-2,4-Diamine-Functionalized Magnetic Nanoparticles: Applied for Synthesis of 1,4-Dihydropyridine Pharmaceutical Derivatives. Ultrason. Sonochem. 2019, 59, 104737. DOI: 10.1016/j.ultsonch.2019.104737.
- Babu, S. G.; Karthik, P.; John, M. C.; Lakhera, S. K.; Ashokkumar, M.; Khim, J.; Neppolian, B. Synergistic Effect of Sono-Photocatalytic Process for the Degradation of Organic Pollutants Using CuO-TiO2/RGO. Ultrason. Sonochem. 2019, 50, 218–223. DOI: 10.1016/j.ultsonch.2018.09.021.
- Sumitomo, S.; Koizumi, H.; Uddin, M. A.; Kato, Y. Comparison of Dispersion Behavior of Agglomerated Particles in Liquid between Ultrasonic Irradiation and Mechanical Stirring. Ultrason. Sonochem. 2018, 40, 822–831. DOI: 10.1016/j.ultsonch.2017.08.023.
- Hebishy, A. M. S.; Abdelfattah, M. S.; Elmorsy, A.; Elwahy, A. H. M. ZnO Nanoparticles Catalyzed Synthesis of Bis- and Poly(Imidazoles) as Potential Anticancer Agents. Synth. Commun. 2020, 50, 980–996. DOI: 10.1080/00397911.2020.1726396.
- Shehab, W. S.; EL-Farargy, A. F.; Abdelhamid, A. O.; Aziz, M. A. Synthesis and Biological Application of Pyranopyrimidine Derivatives Catalyzed by Efficient Nanoparticles and Their Nucleoside Analogues. Synth. Commun. 2019, 49, 3560–3572. DOI: 10.1080/00397911.2019.1679538.
- Nasrollahzadeh, M.; Atarod, M.; Sajjadi, M.; Sajadi, S. M.; Issaabadi, Z. Chapter 6 - Plant-Mediated Green Synthesis of Nanostructures: Mechanisms, Characterization, and Applications. In An Introduction to Green Nanotechnology; Nasrollahzadeh, M., Sajadi, S. M., Sajjadi, M., Issaabadi, Z., Atarod, M., Eds.; Elsevier: London, 2019; Vol. 28, pp 199–322. DOI: 10.1016/B978-0-12-813586-0.00006-7.
- Tosun, F.; Kizilay, C. A. Anthraquinones and Flavonoids from Rheum Ribes. J. Fac. Pharm. Ankara. 2003, 32, 31–35.
- Kaur, N. Synthesis of Six- and Seven-Membered Heterocycles under Ultrasound Irradiation. Synth. Commun. 2018, 48, 1235–1258. DOI: 10.1080/00397911.2018.1434894.
- Kaur, N. Ultrasound-Assisted Green Synthesis of Five-Membered O- and S-Heterocycles. Synth. Commun. 2018, 48, 1715–1738. DOI: 10.1080/00397911.2018.1460671.
- Nikpassand, M.; Fekri, L. Z.; Nabatzadeh, M. Efficient and Green Synthesis of Novel Derivatives of 3,3′-((Aryl-1-Phenyl-1H-Pyrazol-4-Yl)Methylene)Bis(1H-Indole) under Ultrasound Irradiation. Synth. Commun. 2017, 47, 29–36. DOI: 10.1080/00397911.2016.1249286.
- Wang, X.; Wei, Y.; Wang, J.; Guo, W.; Wang, C. The Kinetics and Mechanism of Ultrasonic Degradation of P-Nitrophenol in Aqueous Solution with CCl4 Enhancement. Ultrason. Sonochem. 2012, 19, 32–37. DOI: 10.1016/j.ultsonch.2010.12.005.
- Atarod, M.; Safari, J. Synergistic Effect between Ultrasound Irradiation and Na2CO3 in N-Acylation Reaction: Applied for the Synthesis of Novel N-Acylcyanamide Derivatives. ChemistrySelect. 2020, 5, 2219–2224. DOI: 10.1002/slct.201904793.
- Yella, R.; Khatun, N.; Rout, S. K.; Patel, B. K. Tandem Regioselective Synthesis of Tetrazoles and Related Heterocycles Using Iodine. Org. Biomol. Chem. 2011, 9, 3235–3245. DOI: 10.1039/C0OB01007C.
- Voitekhovich, S. V.; Vorob'ev, A. N.; Gaponik, P. N.; Ivashkevich, O. A. Synthesis of New Functionally Substituted 1-R-Tetrazoles and Their 5-Amino Derivatives. Chem. Heterocycl. Compd. 2005, 41, 999–1004. DOI: 10.1007/s10593-005-0267-4.