References
- Woo, G. H. C.; Snyder, J. K.; Wan, Z.-K. Prog. Heterocycl. Chem. 2002, 7, 279–309.
- Krbavcic, A. The Chemistry of Heterocyclic Compounds, Vol. 47, E.C. Taylor, Editor, the Synthesis of Heterocycles, Part 2, G.P. Ellis, John Wiley & Sons LTD, Cardiff UK, 1992, 160 Engl. £. Arch. Pharm. Pharm. Med. Chem. 1994, 327, 198–198. DOI: https://doi.org/10.1002/ardp.19943270317.
- Kurasawa, Y.; Sakata, G.; Makino, K. Recent Progress in the Quinoline Chemistry. Synthesis and Biological Activity. Heterocycles 1988, 27, 2481. DOI: https://doi.org/10.3987/REV-88-397.
- Darkins, P.; McCarthy, N.; McKervey, M. A.; Ye, T. Oxidation of α-Diazoketones Derived from L -Amino Acids and Dipeptides Using Dimethyldioxirane. Synthesis and Reactions of Homochiral N-Protected α-Amino Glyoxals. J. Chem. Soc. Chem. Commun. 1993, 98, 1222–1223. DOI: https://doi.org/10.1039/C39930001222.
- Hegedus, L. S.; Greenberg, M. M.; Wendling, J. J.; Bullock, J. P. Synthesis of 5,12-Dioxocyclam Nickel (II) Complexes Having Quinoxaline Substituents at the 6 and 13 Positions as Potential DNA Bis-Intercalating and Cleaving Agents. J. Org. Chem. 2003, 68, 4179–4188. DOI: https://doi.org/10.1021/jo020708r.
- Justin Thomas, K. R.; Velusamy, M.; Lin, J. T.; Chuen, C.; Tao, Y.-T. Chromophore-Labeled Quinoxaline Derivatives as Efficient Electroluminescent Materials. Chem. Mater. 2005, 17, 1860–1866. DOI: https://doi.org/10.1021/cm047705a.
- O’Brien, D.; Weaver, M. S.; Lidzey, D. G.; Bradley, D. D. C. Use of Poly(Phenyl Quinoxaline) as an Electron Transport Material in Polymer Light-Emitting Diodes. Appl. Phys. Lett. 1996, 69, 881–883. DOI: https://doi.org/10.1063/1.117975.
- Lee, K.-H. Anticancer Drug Design Based on Plant-Derived Natural Products. J. Biomed. Sci. 1999, 6, 236–250. DOI: https://doi.org/10.1007/BF02253565.
- Xekoukoulotakis, N.; Hadjiantoniou-Maroulis, C.; Maroulis, A. Synthesis of Quinoxalines by Cyclization of α-Arylimino Oximes of α-Dicarbonyl Compounds. Tetrahedron Lett. 2000, 41, 10299–10302. DOI: https://doi.org/10.1016/S0040-4039(00)01847-5.
- Islami, M. R.; Hassani, Z. One-Pot and Efficient Protocol for Synthesis of Quinoxaline Derivatives. Arkivoc 2008, 2008, 280–287. DOI: https://doi.org/10.3998/ark.5550190.0009.f24.
- Naresh, G.; Kant, R.; Narender, T. Copper(II) Catalyzed Expeditious Synthesis of Furoquinoxalines through a One-Pot Three-Component Coupling Strategy. Org. Lett. 2014, 16, 4528–4531. DOI: https://doi.org/10.1021/ol502072k.
- Heravi, M. M.; Taheri, S.; Bakhtiari, K.; Oskooie, H. A. On Water: A Practical and Efficient Synthesis of Quinoxaline Derivatives Catalyzed by CuSO4·5H2O. Catal. Commun. 2007, 8, 211–214. DOI: https://doi.org/10.1016/j.catcom.2006.06.013.
- Tarpada, U. P.; Thummar, B. B.; Raval, D. K. A Green Protocol for the Synthesis of Quinoxaline Derivatives Catalyzed by Polymer Supported Sulphanilic Acid. Arab. J. Chem. 2017, 10, S2902–S2907. DOI: https://doi.org/10.1016/j.arabjc.2013.11.021.
- Niknam, K.; Saberi, D.; Mohagheghnejad, M. Silica Bonded S-Sulfonic Acid: A Recyclable Catalyst for the Synthesis of Quinoxalines at Room Temperature. Molecules 2009, 14, 1915–1926. DOI: https://doi.org/10.3390/molecules14051915.
- Yelwande, A. A.; Navgire, M. E.; Arbad, B. R.; Lande, M. K. Polyaniline/SiO2 Nanocomposite Catalyzed Efficient Synthesis of Quinoxaline Derivatives at Room Temperature. J. Chinese Chem. Soc. 2012, 59, 995–1000. DOI: https://doi.org/10.1002/jccs.201100482.
- Kotharkar, S. A.; Shinde, D. B. Lead Oxide (PbO) Mediated Synthesis of Quinoxaline. JICS 2006, 3, 267–271. DOI: https://doi.org/10.1007/BF03247218.
- Rashidizadeh, G. Proceedings 2019, 9, 49.
- Cai, J. J.; Zou, J. P.; Pan, X. Q.; Zhang, W. Gallium(III) Triflate-Catalyzed Synthesis of Quinoxaline Derivatives. Tetrahedron Lett. 2008, 49, 7386–7390. DOI: https://doi.org/10.1016/j.tetlet.2008.10.058.
- Huang, T. k.; Wang, R.; Shi, L.; Lu, X. x. Montmorillonite K-10: An Efficient and Reusable Catalyst for the Synthesis of Quinoxaline Derivatives in Water. Catal. Commun. 2008, 9, 1143–1147. DOI: https://doi.org/10.1016/j.catcom.2007.10.024.
- Kozhevnikov, I. V.; Matveev, K. I. Homogeneous Catalysts Based on Heteropoly Acids (Review). Appl. Catal. 1983, 5, 135–150. DOI: https://doi.org/10.1016/0166-9834(83)80128-6.
- Rafiee, E.; Eavani, S. Heterogenization of Heteropoly Compounds: A Review of Their Structure and Synthesis. RSC Adv. 2016, 6, 46433–46466. DOI: https://doi.org/10.1039/C6RA04891A.
- Yu, F. L.; Liu, C. Y.; Xie, P. H.; Yuan, B.; Xie, C. X.; Yu, S. T. Oxidative-Extractive Deep Desulfurization of Gasoline by Functionalized Heteropoly Acid Catalysts. RSC Adv. 2015, 5, 85540–85546. DOI: https://doi.org/10.1039/C5RA16013H.
- Farhadi, S.; Hakimi, M.; Maleki, M. 12-Molybdophosphoric Acid Anchored on Aminopropylsilanized Magnetic Graphene Oxide Nanosheets (Fe3O4/GrOSi(CH2)3-NH2/H3PMo12O40): A Novel Magnetically Recoverable Solid Catalyst for H2O2-Mediated Oxidation of Benzylic Alcohols under Solvent-Free Conditions. RSC Adv. 2018, 8, 6768–6780. DOI: https://doi.org/10.1039/c8ra00312b.
- Heravi, M. M.; Vazin Fard, M.; Faghihi, Z. Heteropoly Acids-Catalyzed Organic Reactions in Water: Doubly Green Reactions. Green Chem. Lett. Rev. 2013, 6, 282–300. DOI: https://doi.org/10.1080/17518253.2013.846415.
- Chavan, L. D.; Shankarwar, S. G. KSF Supported 10-Molybdo-2-Vanadophosphoric Acid as an Efficient and Reusable Catalyst for One-Pot Synthesis of 2,4,5-Trisubstituted Imidazole Derivatives under Solvent-Free Condition. Chinese J. Catal. 2015, 36, 1054–1059. DOI: https://doi.org/10.1016/S1872-2067(15)60830-0.
- Chavan, L. D.; Nagolkar, B. B.; Chondhekar, T. K.; Shankarwar, S. G. Orbital Electron. J. Chem. 2017, 9, 210–218. DOI: https://doi.org/10.17807/orbital.v9i4.873.
- Wu, H.; Zhou, M.; Qu, Y.; Li, H.; Yin, H. Preparation and Characterization of Tungsten-Substituted Molybdophosphoric Acids and Catalytic Cyclodehydration of 1,4-Butanediol to Tetrahydrofuran. Chinese J. Chem. Eng. 2009, 17, 200–206. DOI: https://doi.org/10.1016/S1004-9541(08)60194-9.
- Cai, H.; Wu, X.; Wu, Q.; Yan, W. Synthesis and High Proton Conductive Performance of a Quaternary Vanadomolybdotungstosilicic Heteropoly Acid. Dalton Trans. 2016, 45, 14238–14242. DOI: https://doi.org/10.1039/c6dt02727j.
- Farhadi, S.; Zareisahamieh, R.; Zaidi, M. H6GeMo10V2O40·16H2O Nanoparticles Prepared by Hydrothermal Method: A New and Reusable Heteropoly Acid Catalyst for Highly Efficient Acetylation of Alcohols and Phenols under Solvent-Free Conditions. J. Braz. Chem. Soc. 2011, 22, 1323–1332. DOI: https://doi.org/10.1590/S0103-50532011000700018.
- Xie, Z.; Wu, H.; Wu, Q.; Ai, L. Synthesis and Performance of Solid Proton Conductor Molybdovanadosilicic Acid. RSC Adv. 2018, 8, 13984–13988. DOI: https://doi.org/10.1039/c8ra02390e.
- Aher, D. S.; Khillare, K. R.; Chavan, L. D.; Shankarwar, S. G. Tungsten-Substituted Molybdophosphoric Acid Impregnated with Kaolin: Effective Catalysts for the Synthesis of 3,4-Dihydropyrimidin-2(1H)-Ones via Biginelli Reaction. RSC Adv. 2021, 11, 2783–2792. DOI: https://doi.org/10.1039/d0ra09811f.
- Aher, D. S.; Khillare, K. R.; Shankarwar, S. G. Incorporation of Keggin-Based H3PW7Mo5O40 into Bentonite: Synthesis, Characterization and Catalytic Applications. RSC Adv. 2021, 11, 11244–11254. DOI: https://doi.org/10.1039/d1ra01179k.
- Aher, D. S.; Khillare, K. R.; Chavan, L. D.; Shankarwar, S. G. Quaternary Vanado‐Molybdotungstophosphoric Acid [H5PW6Mo4V2O40] over Natural Montmorillonite as a Heterogeneous Catalyst for the Synthesis 4H-Pyran and Polyhydroquinoline Derivatives. ChemistrySelect 2020, 5, 7320–7331. DOI: https://doi.org/10.1002/slct.202001065.
- Khillare, K. R.; Aher, D. S.; Chavan, L. D.; Shankarwar, S. G. Cesium Salt of 2-Molybdo-10-Tungstophosphoric Acid as an Efficient and Reusable Catalyst for the Synthesis of Uracil Derivatives via a Green Route. RSC Adv. 2021, 11, 33980–33989. DOI: https://doi.org/10.1039/d1ra05190c.
- Aher, D. S.; Khillare, K. R.; Chavan, L. D.; Shankarwar, S. G. H3PMo7W5O40·24H2O Catalyzed Access to Fused Pyrazolopyranopyrimidine Derivatives via One-Pot Multicomponent Synthesis: Green Chemistry. Monatsh. Chem. 2022, 153, 79–85. DOI: https://doi.org/10.1007/s00706-021-02868-7.
- Ruiz, D. M.; Autino, J. C.; Quaranta, N.; Vázquez, P. G.; Romanelli, G. P. An Efficient Protocol for the Synthesis of Quinoxaline Derivatives at Room Temperature Using Recyclable Alumina-Supported Heteropolyoxometalates. Sci. World J. 2012, 2012, 1–8. DOI: https://doi.org/10.1100/2012/174784.
- Chandrachood, P. S.; Jadhav, A. R.; Garud, D. R.; Deshpande, N. R.; Puranik, V. G.; Kashalkar, R. V. An Efficient Method for the Synthesis of Quinoxaline Derivatives Catalyzed by Titanium Silicate-1. Res. Chem. Intermed. 2020, 46, 5219–5230. DOI: https://doi.org/10.1007/s11164-020-04258-w.
- Raw, S. A.; Wilfred, C. D.; Taylor, R. J. K. Tandem Oxidation Processes for the Preparation of Nitrogen-Containing Heteroaromatic and Heterocyclic Compounds. Org. Biomol. Chem. 2004, 2, 788–796. DOI: https://doi.org/10.1039/b315689c.