Ali, M.M., Ismail, M.M.F., El-Gaby, M.S.A., Zahran, M.A., and Ammar, Y.A., 2000. Synthesis and antimicrobial activities of some novel quinoxalinone derivatives. Molecules. 5(6), 864–873.
Arabpoor, Z., and Shaterian, H.R., 2016. l-Leucine supported on superparamagnetic silica-encapsulated γ-Fe2O3 nanoparticles: design, characterization, and application as a green catalyst for highly efficient synthesis of thiazoloquinolines. RSC Advances. 6(50), 44459–44468.
Azizi, K., and Heydari, A., 2014. Vitamin B1 supported on silica-encapsulated γ-Fe2O3 nanoparticles: design, characterization and application as a greener biocatalyst for highly efficient acylation. RSC Advances. 4(17), 8812–8816.
Azizi, K., Karimi, M., Shaterian, H.R., and Heydari, A., 2014. Ultrasound irradiation for the green synthesis of chromenes using L-arginine-functionalized magnetic nanoparticles as a recyclable organocatalyst. RSC Advances. 4(79), 42220–42225.
Bathaie, S.Z., Bolhasani, A., Hoshyar, R., Ranjbar, B., Sabouni, F., and Moosavi-Movahedi, A.A., 2007. Interaction of saffron carotenoids as anticancer compounds with ctDNA, Oligo (dG. dC) 15, and Oligo (dA. dT) 15. DNA and Cell Biology. 26(8), 533–540.
Clark, J.H., Budarin, V., Deswarte, F.E.I., Hardy, J.J.E., Kerton, F.M., Hunt, A.J.,
Luque, R.,
Macquarrie, D.J.,
Milkowski, K.,
Rodriguez, A.,
Samuel, O.,
Tavener, S.J.,
White, R.J., and
Wilson, A.J., 2006. Green chemistry and the biorefinery: a partnership for a sustainable future. Green Chemistry. 8(10), 853–860.
Crossley, M.J., and Johnston, L.A., 2002. Laterally-extended porphyrin systems incorporating a switchable unit. Chemical Communication. (10), 1122–1123.
Dailey, S., Feast, W.J., Peace, R.J., Sage, I.C., Till, S., and Wood, E.L., 2001. Synthesis and device characterisation of side-chain polymer electron transport materials for organic semiconductor applications. Journal of Materials Chemistry. 11(9), 2238–2243.
Escribano, J., Alonso, G.L., Coca-Prados, M., and Fernández, J.A., 1996. Crocin, safranal and picrocrocin from saffron (Crocus sativus L.) inhibit the growth of human cancer cells in vitro. Cancer Letters. 100(1–2), 23–30.
Huang, Y., and Zhang, W., 2013. Magnetic nanoparticle-supported organocatalysis. Green Processing and Synthesis. 2(6), 603–609.
Jafarpour, M., Rezaeifard, A., and Danehchin, M., 2011. Easy access to quinoxaline derivatives using alumina as an effective and reusable catalyst under solvent-free conditions. Applied Catalysis A: General. 394(1), 48–51.
Jafarpour, M., Rezaeifard, A., Gazkar, S., and Danehchin, M., 2011. Catalytic activity of a zirconium (IV) Schiff base complex in facile and highly efficient synthesis of indole derivatives. Transition Metal Chemistry. 36(7), 685.
Jafarpour, M., Rezaeifard, A., Ghahramaninezhad, M., and Tabibi, T., 2013. Reusable α-MoO3 nanobelts catalyzes the green and heterogeneous condensation of 1, 2-diamines with carbonyl compounds. New Journal of Chemistry. 37(7), 2087–2095.
Jafarpour, M., Rezaeifard, A., and Golshani, T., 2009. A new catalytic method for ecofriendly synthesis of bis-and trisindolylmethanes by zirconyldodecylsulfate under mild conditions. Journal of Heterocyclic Chemistry. 46(3), 535–539.
Jafarpour, M., Rezaeifard, A., and Gorzin, G., 2011. Enhanced catalytic activity of Zr (IV) complex with simple tetradentate Schiff base ligand in the clean synthesis of indole derivatives. Inorganic Chemistry Communications. 14(11), 1732–1736.
Jafarpour, M., Rezaeifard, A., Haddad, R., and Gazkar, S., 2013. A reusable zirconium (IV) Schiff base complex catalyzes highly efficient synthesis of quinoxalines under mild conditions. Transition Metal Chemistry. 38(1), 31–36.
Jafarpour, M., Rezaeifard, A., and Heidari, M., 2011. A new catalytic method for eco-friendly synthesis of quinoxalines by zirconium (IV) oxide chloride octahydrate under mild conditions. Letters in Organic Chemistry. 8(3), 202–209.
Jafarpour, M., Rezapour, E., Ghahramaninezhad, M., and Rezaeifard, A., 2014. A novel protocol for selective synthesis of monoclinic zirconia nanoparticles as a heterogeneous catalyst for condensation of 1, 2-diamines with 1, 2-dicarbonyl compounds. New Journal of Chemistry. 38(2), 676–682.
Justin Thomas, K.R., Velusamy, M., Lin, J.T., Chuen, C.H., and Tao, Y.T., 2005. Chromophore-labeled quinoxaline derivatives as efficient electroluminescent materials. Chemistry of Materials. 17(7), 1860–1866.
Kanakis, C.D., Tarantilis, P.A., Pappas, C., Bariyanga, J., Tajmir-Riahi, H.A., and Polissiou, M.G., 2009. An overview of structural features of DNA and RNA complexes with saffron compounds: Models and antioxidant activity. Journal of Photochemistry and Photobiology B: Biology. 95(3), 204–212.
Khaksarnezhad, E., and Zabet, M., 2017. The effect of nano iron chelated on the yield and yield components of saffron (Crocus sativus L.) in South Khorasan. Journal of Saffron Research. 5(1), 45-52. [In Persian with English Summary].
Mizuno, T., Wei, W.H., Eller, L.R., and Sessler, J.L., 2002. Phenanthroline complexes bearing fused dipyrrolylquinoxaline anion recognition sites: efficient fluoride anion receptors. Journal of the American Chemical Society. 124(7), 1134–1135.
Subran, S.K., and Paira, P., 2017. Synthesis and pharmacological applications of certain quinoxaline analogues: A review. Current Bioactive Compounds. 13(3), 186–212.
Tang, B.Z., Geng, Y., Lam, J.W.Y., Li, B., Jing, X., Wang, X., and Zhang, X.X., 1999. Processible nanostructured materials with electrical conductivity and magnetic susceptibility: preparation and properties of maghemite/polyaniline nanocomposite films. Chemistry of Materials. 11(6), 1581–1589.
Yang, H., Li, S., Wang, X., Zhang, F., Zhong, X., Dong, Z., and Ma, J., 2012. Core-shell silica magnetic microspheres supported proline as a recyclable organocatalyst for the asymmetric aldol reaction. Journal of Molecular Catalysis A: Chemical. 363, 404–410.