References
- Senkiv J, Finiuk N, Kaminskyy D, et al. 5-Ene-4-thiazolidinones induce apoptosis in mammalian leukemia cells. Eur J Med Chem. 2016;117:33–46. doi: 10.1016/j.ejmech.2016.03.089
- Ashour HMA, El-Ashmawy IM, Bayad AE. Synthesis and pharmacological evaluation of new pyrazolyl benzenesulfonamides linked to polysubstituted pyrazoles and thiazolidinones as anti-inflammatory and analgesic agents. Monatsh Chem. 2016;147:605–618. doi: 10.1007/s00706-015-1549-x
- Nechak R, Bouzroura SA, Benmalek Y, et al. Synthesis and antimicrobial activity evaluation of novel 4-thiazolidinones containing a pyrone moiety. Synth Commun. 2015;45:262–272. doi: 10.1080/00397911.2014.970278
- Subhedar DD, Shaikh MH, Arkile MA, et al. Facile synthesis of 1,3-thiazolidin-4-ones as antitubercular agents. Bioorg Med Chem Lett. 2016;26:1704–1708. doi: 10.1016/j.bmcl.2016.02.056
- Havrylyuk D, Zimenkovsky B, Vasylenko O, et al. Synthesis and anticancer and antiviral activities of new 2-pyrazoline-substituted 4-thiazolidinones. J Heterocyclic Chem. 2013;50:E55–E62. doi: 10.1002/jhet.1056
- Rawal RK, Prabhakar YS, Katti SB, et al. 2-(Aryl)-3-furan-2-ylmethyl-thiazolidin-4-ones as selective HIV-RT inhibitors. Bioorg Med Chem Lett. 2005;13:6771–6776. doi: 10.1016/j.bmc.2005.07.063
- Rawal RK, Tripathi R, Katti SB, et al. Design, synthesis, and evaluation of 2-aryl-3-heteroaryl-1,3-thiazolidin-4-ones as anti-HIV agents. Bioorg Med Chem. 2007;15:1725–1731. doi: 10.1016/j.bmc.2006.12.003
- Kumar D, Sonawane M, Pujala B, et al. Supported protic acid-catalyzed syntheis of 2,3-disubstituted thiazolidin-4-ones: enhancement of the catalytic potential of protic acid by adsorption on solid supports. Green Chem. 2013;15:2872–2884. doi: 10.1039/c3gc41218k
- Meshram J, Ali P, Tiwari V. Zeolite as an efficient and recyclable activation surface for the synthesis of bis thiazolidinones: theoretical screening owing to experimental biology. Green Chem Lett Rev. 2010;3:195–200. doi: 10.1080/17518251003660154
- Mobinikhaledi A, Amiri AK. Green and highly efficient one-pot synthesis of some new bis thiazolidinones. Lett Org Chem. 2013;10:764–769. doi: 10.2174/157017861131000059
- Abdel-Rahman RM, Ali TE. Synthesis and biological evaluation of some new polyfluorinated 4-thiazolidinone and a-aminophosphonic acid derivatives. Monatsh Chem. 2013;144:1243–1252. doi: 10.1007/s00706-013-0934-6
- Safaei-Ghomi J, Asgari-Keirabadi M, Khojastehbakht-Koopaei B, et al. Multicomponent synthesis of C-tethered bispyrazol-5-ols using CeO2 nanoparticles as an efficient and Green catalyst. Res Chem Intermed. 2016;42:827–837. doi: 10.1007/s11164-015-2057-7
- Safaei-Ghomi J, Kiani M, Ziarati A, et al. Highly efficient synthesis of benzopyranopyridines via ZrP2O7 nanoparticles catalyzed multicomponent reactions of salicylaldehydes with malononitrile and thiols. J Sulfur Chem. 2014;35:450–457. doi: 10.1080/17415993.2014.913291
- Shil AK, Das P. Polystyrene resin supported palladium(0) (Pd@PR) nanocomposite catalyzed synthesis of β-aryl and β,β-diaryl unsaturated scaffolds following tandem approaches. RSC Adv. 2015;5:24859–24863. doi: 10.1039/C5RA00228A
- Maddila S, Rana S, Pagadala R, et al. Synthesis of pyrazole-4-carbonitrile derivatives in aqueous media with CuO/ZrO2 as recyclable catalyst. Catal Commun. 2015;61:26–30. doi: 10.1016/j.catcom.2014.12.005
- Sharma RK, Dutta S, Sharma S, et al. Fe3O4 (iron oxide)-supported nanocatalysts: synthesis, characterization and applications in coupling reactions. Green Chem. 2016;18:3184–3209. doi: 10.1039/C6GC00864J
- Safaei-Ghomi J, Nazemzadeh SH, Shahbazi-Alavi H. Novel magnetic nanoparticles-supported inorganic-organic hybrids based on POSS as an efficient nanomagnetic catalyst for the synthesis of pyran derivatives. Catal Commun. 2016;86:14–18. doi: 10.1016/j.catcom.2016.07.022
- Safaei-Ghomi J, Navvab M, Shahbazi-Alavi H. Cofe2o4@SiO2/PrNH2 nanoparticles as highly efficient and magnetically recoverable catalyst for the synthesis of 1,3-thiazolidin-4-ones. J Sulfur Chem. 2016. DOI: 10.1080/17415993.2016.1169533
- Safaei-Ghomi J, Babaei P, Shahbazi-Alavi H, et al. A concise synthesis of furo[3,2-c]coumarins catalyzed by nanocrystalline ZnZr4(PO4)6 ceramics under microwave irradiation. J Iran Chem Soc. 2016;13:1439–1448. doi: 10.1007/s13738-016-0859-1
- Previtera T, Basile M, Vigorita MG, et al. 3,3′-Di[1,3-thiazolidine-4-one] system. II. Anti-Inflammatory and Anti-Histaminic Properties in new Substituted Derivatives. Eur J Med Chem. 1987;22:67–74. doi: 10.1016/0223-5234(87)90175-9
- Kouznetsov VV, Amado DF, Bahsas A, et al. Synthesis and spectral data of new 1,2-bis-(2-hetaryl-4-oxothiazolidin-3-yl)ethanes and 1,4-bis-(2-hetaryl-4-oxothiazolidin-3-yl)butanes. J Heterocyclic Chem. 2006;43:447–452. doi: 10.1002/jhet.5570430228
- Vigorita MG, Previtera T, Ottana R, et al. 3,3′-Bi(1,3-thiazolidin-4-one) system. VIII. 3,3′-(1,2-ethanediyl) derivatives and corresponding 1,1′-disulfones: synthesis, stereochemistry and antiinflammatory activity. Il Farmaco. 1997;52:43–48.
- Safaei-Ghomi J, Shahbazi-Alavi H, Ziarati A. A comparative screening of the catalytic activity of nanocrystalline MIIZr4(PO4)6 ceramics in the one-pot synthesis of 1,6-diamino-4-aryl-2-oxo-1,2-dihydropyridine-3,5-dicarbonitrile derivatives. Res Chem Intermed. 2016. DOI: 10.1007/s11164-016-2608-6