Uncapped SnO2 quantum dot catalyzed cascade assembling of four components: A rapid and green approach to the pyrano[2,3-c]pyrazole and spiro-2-oxindole derivatives

Tetrahedron

Volumn 70, Issue 36, 2014, Pages 6088-6099

  Paul, Sanjay ^a   Pradhan, Koyel ^a   Ghosh, Sirshendu ^b   De, S K ^b   Das, Asish R ^a  

^a UNIVERSITY OF CALCUTTA   (India)

^b DEPARTMENT OF MATERIALS SCIENCE   (India)

Author keywords

Nanoflower; Pyrano 2 3 c pyrazole; Quantum dots; Spiro 2 oxindole

Indexed keywords

INDOLE DERIVATIVE; METAL NANOPARTICLE; OLEIC ACID; PYRANO[2,3 C]PYRAZOLE DERIVATIVE; PYRAZOLE DERIVATIVE; QUANTUM DOT; SPIRO 2 OXINDOLE DERIVATIVE; TIN OXIDE; UNCLASSIFIED DRUG;

ARTICLE; CATALYST; CRYSTAL STRUCTURE; DRUG SYNTHESIS; FIELD EMISSION SCANNING ELECTRON MICROSCOPY; GREEN CHEMISTRY; PARTICLE SIZE; PRIORITY JOURNAL; RECYCLING; TRANSMISSION ELECTRON MICROSCOPY; X RAY DIFFRACTION;

EID: 84949116866     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2014.02.077     Document Type: Article

References (49)

1. S. Mandal, D. Roy, R.V. Chaudhari, and M. Sastry Chem. Mater. 16 2004 3714
2. R. Tatumi, T. Akita, and H. Fujihara Chem. Commun. 2006 3349
3. A.M. White, A.J. Johnson, T.J. Koberstein, and N.J. Turro J. Am. Chem. Soc. 128 2006 11356
4. Y. Niu, K.L. Yeung, and R.M. Crooks J. Am. Chem. Soc. 123 2001 6840
5. W. Teunissen, A.A. Bol, and J.W. Geus Catal. Today 48 1999 329
6. W.P. Smith, L.S. Sollis, D.P. Howes, C.P. Cherry, D.I. Starkey, and N.K. Cobley J. Med. Chem. 41 1998 787
7. K. Mazaahir, S. Shilpi, R.K. Khalilur, and S.T. Sharanjit Bioorg. Med. Chem. Lett. 15 2005 4295
8. J.L. Wang, D. Liu, Z.J. Zheng, S. Shan, X. Han, S.M. Srinivasula, C.M. Croce, E.S. Alnemri, and Z. Huang Proc. Natl. Acad. Sci. U.S.A. 97 2009 7124
9. M.E.A. Zaki, E.M. Morsy, and M. Abdul Heterocycl. Commun. 10 2004 97
10. M.E.A. Zaki, H.A. Saliman, O.A. Hickal, and A.E. Rashad Z. Naturforsch., C: Biosci. 61 2006 1
11. C.K. Sheng, J.H. Li, and N. Hideo J. Med. Chem. 27 1984 539
12. N. Foloppe, L.M. Fisher, R. Howes, A. Potter, A.G.S. Robertson, and A.E. Surgenor Bioorg. Med. Chem. 14 2006 4792
13. H. Junek, and H. Aigner Chem. Ber. 106 1973 914
14. H. Wamhoff, E. Kroth, and K. Strauch Synthesis 11 1993 1129
15. A.V. Stachulski, N.G. Berry, A.C.L. Low, S.L. Moores, E. Row, D.C. Warhurst, I.S. Adagu, and J.F. Rossignol J. Med. Chem. 49 2006 1450
16. W.J. Houlihan, W.A. Remers, and R.K. Brown Indoles: Part I 1992 Wiley New York, NY
17. R.J. Sundberg The Chemistry of Indoles 1996 Academic New York, NY
18. J.F.M. Da-Silva, S.J. Garden, and A.C. Pinto J. Braz. Chem. Soc. 12 2001 273
19. K.C. Joshi, and P. Chand Pharmazie 37 1982 1
20. K.C. Joshi, R. Jain, and K. Sharma J. Indian Chem. Soc. 115 1988 202
21. A.H. Abdel-Rahman, E.M. Keshk, M.A. Hanna, and Sh M. El-Bady Bioorg. Med. Chem. 12 2004 2483
22. A. Dandia, R. Singh, S. Khaturia, C. Merienne, G. Morgant, and A. Loupy Bioorg. Med. Chem. 14 2006 2409
23. M.M. Khafagy, A.H.F.A. El-Wahas, F.A. Eid, and A.M. El-Agrody Farmaco 57 2002 715
24. P.R. Sebahar, and R.M. Williams J. Am. Chem. Soc. 122 2000 5666
25. J. Ma, and S.M. Hecht Chem. Commun. 2004 1190
26. S. Edmondson, S.J. Danishefsky, L. Sepp-lorenzinol, and N. Rosen J. Am. Chem. Soc. 121 1999 2147
27. T.H. Kang, K. Matsumoto, Y. Murakami, H. Takayama, M. Kitajima, N. Aimi, and H. Watanabe Eur. J. Pharmacol. 444 2002 39
28. D.J. Ramon, and M. Yus Angew. Chem., Int. Ed. 44 2005 1602
29. J. Zhu Eur. J. Org. Chem. 2003 1133
30. I. Ugi, A. Domling, and B. Werner J. Heterocycl. Chem. 37 2000 647
31. H. Bienayme, C. Hulme, G. Oddon, and P. Schmitt Chem. - Eur. J. 6 2000 3321
32. V.S. Shinu, B. Sheeja, E. Purushothaman, and D. Bahulayan Tetrahedron Lett. 50 2009 4838
33. V.A. Chebanov, E.A. Muravyova, S.M. Desenko, V.I. Musatov, I.V. Knyazeva, S.V. Shishkina, O.V. Shishkin, and C.O. Kappe J. Comb. Chem. 8 2006 427
34. A. Dondoni, A. Massi, S. Sabbatini, and V. Bertolasi J. Org. Chem. 67 2002 6979
35. G. Rashinkar, and R. Salunkhe J. Mol. Catal. A: Chem. 316 2010 146
36. L. Xiao, H. Shen, R. von Hagen, J. Pan, L. Belkoura, and S. Mathur Chem. Commun. 2010 6509
37. T.T. Baby, and S. Ramaprabhu J. Appl. Phys. 111 2012 034311
38. H. Ahn, H. Choi, K. Park, S. Kim, and Y.J. Sung Phys. Chem. B 108 2004 9815
39. T. Jia, W. Wang, F. Long, Z. Fu, H. Wang, and Q. Zhang J. Phys. Chem. C 113 2009 9071
40. S. Gubbala, V. Chakrapani, V. Kumar, and M.K. Sunkara Adv. Funct. Mater. 18 2008 2411
41. N. Kudo, Y. Shimazaki, H. Ohkita, M. Ohoka, and S. Ito Sol. Energy Mater. Sol. Cells 91 2007 1243
42. S. Paul, P. Bhattacharyya, and A.R. Das Tetrahedron Lett. 52 2011 4636
43. P. Bhattacharyya, K. Pradhan, S. Paul, and A.R. Das Tetrahedron Lett. 53 2012 4687
44. S. Paul, G. Pal, and A.R. Das RSC Adv. 3 2013 8637
45. S. Paul, S. Ghosh, P. Bhattacharyya, and A.R. Das RSC Adv. 3 2013 14254
46. P.P. Ghosh, and A.R. Das Tetrahedron Lett. 25 2012 3140
47. K. Pradhan, S. Paul, and A.R. Das Catal. Sci. Technol. 4 2014 822
48. S. Ghosh, K. Das, K. Chakrabarti, and S.K. De CrystEngComm 14 2012 929
49. S. Ghosh, K. Das, K. Chakrabarti, and S.K. De Dalton Trans. 42 2013 3434