Biological synthesis of ZnO nanoparticles using C. albicans and studying their catalytic performance in the synthesis of steroidal pyrazolines

Arabian Journal of Chemistry

Volumn 10, Issue , 2017, Pages S1530-S1536

  Shamsuzzaman, ^a   Mashrai, Ashraf ^a   Khanam, Hena ^a   Aljawfi, Rezq Naji ^a  

^a ALIGARH MUSLIM UNIVERSITY   (India)

Author keywords

C. albicans; Nanoparticles; Pyrazoline; Steroid; ZnO

Indexed keywords

BIOCHEMISTRY; BIOSYNTHESIS; CANDIDA; DIFFERENTIAL THERMAL ANALYSIS; ELECTRON MICROSCOPY; GRAVIMETRIC ANALYSIS; HIGH RESOLUTION TRANSMISSION ELECTRON MICROSCOPY; KETONES; METAL NANOPARTICLES; MOLECULES; NANOPARTICLES; SCANNING ELECTRON MICROSCOPY; THERMOANALYSIS; THERMOGRAVIMETRIC ANALYSIS; TRANSMISSION ELECTRON MICROSCOPY; X RAY DIFFRACTION; ZINC OXIDE;

ALBICANS; BIOLOGICAL SYNTHESIS; CATALYTIC PERFORMANCE; DIFFERENTIAL THERMAL ANALYSES (DTA); EFFICIENT SYNTHESIS; POWDER X RAY DIFFRACTION; PYRAZOLINES; STEROID;

SYNTHESIS (CHEMICAL);

EID: 84878243348     PISSN: 18785352     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.arabjc.2013.05.004     Document Type: Article

References (39)

1. Abdalla, M.M., Al-Omar, M.A., Bhat, M.A., Amr, A.E., Al-Mohizea, A.M., Int. J. Biol. Macromol. 50 (2012), 1127–1132.
2. Ahn, J.H., Kim, H.M., Jung, S.H., Kang, S.K., Kim, K.R., Rhee, S.D., Yang, S.D., Cheon, H.G., Kim, S.S., Bioorg. Med. Chem. Lett. 14 (2004), 4461–4465.
3. Amir, M., Kumar, H., Khan, S.A., Bioorg. Med. Chem. Lett. 18 (2008), 918–922.
4. Amr, A.E., Hasanien, H.S., Abdalla, M.M., Arch. Pharm. Chem. Life Sci. 338 (2005), 433–440.
5. Bahrami, K., Khodaei, M.M., Nejati, A., Monatsh. Chem. 142 (2011), 159–162.
6. Bansal, E., Srivastava, V.K., Kumar, A., Eur. J. Med. Chem. 36 (2001), 81–92.
7. Bashir, R., Ovais, S., Yaseen, S., Hamid, H., Alam, M.S., Samim, M., Singh, S., Javed, K., Bioorg. Med. Chem. Lett. 21 (2011), 4301–4305.
8. Beydoun, D., Amal, R., Low, G., McEvoy, S., J. Nanopart. Res. 1 (1999), 439–458.
9. Bhacca, N.S., Williams, D.H., Application of NMR Spectroscopy in Organic Chemistry. 1964, Holden Day, San Francisco.
10. Bhattacharyya, P., Pradhan, K., Paul, S., Das, A.R., Tetrahedron Lett. 53 (2012), 4687–4691.
11. Chanaewa, A., Juárez, B.H., Weller, H., Klinke, C., Nanoscale 4 (2012), 251–256.
12. Choudhary, M.I., Alam, M.S., Rahman, A.U., Yousuf, S., Wud, Y.C., Lin, A.S., Shaheen, F., Steroids 76 (2011), 1554–1559.
13. Dauben, W.G., Takemura, K.H., J. Am. Chem. Soc. 75 (1953), 6302–6304.
14. Domling, A., Chem. Rev. 106 (2006), 17–89.
15. Ghomi, J.S., Ghasemzadeh, M.A., Acta Chim. Slov. 59 (2012), 697–702.
16. Gorla, C.R., Emanetoglu, N., Liang, W.S., Mayo, W.E., Lu, Y., Wraback, M., Shen, H., J. Appl. Phys. 85 (1999), 2595–2602.
17. Ha, B., Ham, H., Lee, C.J., J. Phys. Chem. Solids 869 (2000), 2453–2456.
18. Hadjipanayis, G.C., Siegel, R.W., (eds.) Nanophase Mater. Synth. Prop. Appl., 1994, Kluwer, London.
19. Hammam, A.G., Abdel Hafez, N.A., Midura, W.A., Mikolajczyk, M.Z., Naturforsch 55b (2000), 417–424.
20. Havrylyuk, D., Zimenkovsky, B., Vasylenko, O., Gzella, A., Lesyk, R., J. Med. Chem. 55 (2012), 8630–8641.
21. Hosseini, S.M., Sharghi, H., Etemad, S., Helv. Chim. Acta. 91 (2008), 715–724.
22. Ivanyi, Z., Szabo, N., Huber, J., Wölfling, J., Zupko, I., Szecsi, M., Wittmann, T., Schneider, G., Steroids 77 (2012), 566–574.
23. Jayaraj, M.K., Antony, A., Ramachandran, M., Bull. Mater. Sci. 25 (2000), 227–230.
24. Jayaseelan, C., Abdul Rahuman, A., Kirthi, A.V., Marimuthu, S., Santhoshkumar, T., Bagavan, A., Gaurav, K., Karthik, L., Bhaskara Rao, K.V., Spectrochim. Acta Part A 90 (2012), 78–84.
25. Jung, J.C., Watkins, E.B., Avery, M.A., Heterocycles 65 (2005), 77–94.
26. Kantam, M.L., Priyadarshini, S., Joseph, P.J.A., Srinivas, P., Vinu, A., Klabunde, K.J., Nishina, Y., Tetrahedron 68 (2012), 5730–5737.
27. Karthikeyan, M.S., Holla, B.S., Kumari, N.S., Eur. J. Med. Chem. 42 (2007), 30–36.
28. Kim, Y.J., Varma, R.S., Tetrahedron Lett. 45 (2004), 7205–7208.
29. Kumar, A., Gupta, M.K., Kumar, M., Green Chem. 14 (2012), 290–295.
30. Mascolo, G., Agostiano, A., Comparelli, R., Fanizza, E., Curri, M.L., Cozzoli, P.D., Appl. Catal. B Environ. 60 (2005), 1–11.
31. Moghaddam, F.M., Saeidian, H., Mirjafary, H., Sadeghi, A., Catal. Commun. 9 (2008), 299–306.
32. Ni, Y.H., Wei, X.W., Hong, J.M., Ye, Y., Mater. Sci. Eng. B. 121 (2005), 42–47.
33. Palaska, E., Aytemir, M., Uzbay, T., Erol, D., Eur. J. Med. Chem. 36 (2001), 539–543.
34. Rathish, I.G., Javed, K., Ahmad, S., Bano, S., Alam, M.S., Pillai, K.K., Singh, S., Bagchi, V., Bioorg. Med. Chem. Lett. 19 (2009), 255–258.
35. Shamsuzzaman, Khanam, H., Mashrai, A., Siddiqui, N., Tetrahedron Lett. 54 (2013), 874–877.
36. Soares, J.W., Whitten, J.E., Oblas, D.W., Steeves, D.M., Langmuir 24 (2008), 371–374.
37. Tayebee, R., Cheravi, F., Mirzaee, M., Amini, M.M., Chin. J. Chem. 28 (2010), 1247–1252.
38. Xia, Y.N., Yang, P.D., Sun, Y.G., Wu, Y.Y., Mayers, B., Gates, B., Yin, Y.D., Kin, F., Yan, H.Q., Adv. Mater. 15 (2003), 353–389.
39. Zhang, M., Wang, L., Ji, H., Wu, B., Zenge, X., J. Nat. Gas Chem. 16 (2007), 393–417.