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Microwave assisted sulphated titania catalyzed aldol condensation: Synthesis of some (E) 3-(2-naphthyl)-1-(substituted phenyl)-2-propen-1-ones under solvent-free conditions

Treść / Zawartość
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
A series of titled chalcones were synthesized by aldol condensation between 2-naphthaldehyde and various substituted acetophenones using solid acidic solid sulphated titania catalyst under microwave irradiation. The yields of these chalcones are more than 90 %. The synthesized chalcones are characterized by their physical constants, analytical and spectroscopic data.
Rocznik
Tom
Strony
16--22
Opis fizyczny
Bibliogr. 47 poz., tab.
Twórcy
autor
  • Department of Chemistry, National College, Tiruchirappalli - 620 001, India
autor
  • Department of Chemistry, National College, Tiruchirappalli - 620 001, India
  • Department of Chemistry, Annamalai University, Annamalainagar - 608 002, India
Bibliografia
  • [1] Ranganathan K., et al., International Letters of Chemistry, Physics and Astronomy 4 (2012) 66-75.
  • [2] Arulkumaran R., et al., IUP J. Chem. 3(1) (2010) 82-98.
  • [3] Arulkumaran R., Sundararajan R., Vijayakumar S., Sakthinathan S. P., Suresh R., Kamalakkannan D., Ranganathan K., Vanangamudi G., Thirunarayanan G., J. Saudhi Chem. Soc. 2012. Doi: 10.1016/j.jscs.2012.09.006
  • [4] Janaki P., Sekar K. G., Thirunarayanan G., J. Saudi Chem. Soc. 2013. Doi:10.1016/j.jscs.2012.11.013
  • [5] Thirunarayanan G., Vanangamudi G., Subramanian M., Org. Chem.: An Indian Journal 9(1) (2012) 1-16.
  • [6] Sivakumar M., Phrabu Sreeneivasan S., Kumar V., Doble M., Bioorg. Med. Chem. Lett. 17(10) (2007) 3169-3172.
  • [7] Liu X., Go M. L., Bioorg. Med. Chem. 14(1) (2006) 153-163.
  • [8] Arulkumaran R., Sundararajan R., Vanangamudi G., Subramanian M., Ravi K., Sathiyendidran V., Srinivasan S., Thirunarayanan G., IUP J. Chem. 3(1) (2010) 82-98.
  • [9] Deng J., Sanchez T., Lalith Q. A. M., Bioorg. Med. Chem. 15(14) (2007) 4985-5002.
  • [10] Thirunarayanan G., J. Indian Chem. Soc. 84 (2008) 447-451.
  • [11] Thirunarayanan G., Surya S., Srinivasan S., Vanangamudi G., Sathiyendiran V., Spectrochim. Acta 75A (2010) 152-156.
  • [12] Vanangamudi G., Subramanian S., Jayanthi P., Arulkumaran R., Kamalakkannan D., Thirunarayanan G., Arab. J. Chem., 201, DOI:10.1016/j.arabjc.2010.07.019.
  • [13] Tran T. D., Park H., Ecker G. F., Thai K. M., 3,2’-Hydroxychalcone Analogues: Synthesis and Structure-PGE2 Inhibitory Activity Relationship, 12th International Electronic Conference on Synthetic Organic Chemistry (ECSOC-12) 1-30 November 2008;http://www.usc.es/congresos/ecsoc/12/ECSOC12.htm & http://www.mdpi.org/ecsoc-12 No. C0011, pp 1-7.
  • [18] Mohan S. B., Behera T. P., Ravi Kumar B. V. V., Int. J. ChemTech. Res. 2(3) (2010) 1634-1637.
  • [15] Orsini F., Sello G., Fumagalli T., Synlett. 2006, 1717-1718.
  • [16] Thirunarayanan G., Vanangamudi G., Arkivoc. 12 (2006) 58-64.
  • [17] Thirunarayanan G., Ananthakrishna Nadar P., J. Indian Chem. Soc. 83(11) (2006) 1107-1112.
  • [18] Ballini R., Bosica G., Maggi R., Ricciutelli M., Righi P., Sartori G., Sartorio R., Green Chem. 3 (2001) 178-180.
  • [19] Solhy A., Tahir R., Sebti S., Skouta R., Bousmina M., Zahouily M., Larzek M., Appl. Catal. A: General. 374 (2010) 189-193.
  • [20] Basaif S. A., Sobahi T. R., Khalil A. K., Hassan M. A., Bulletin of the Korean Chem. Soc. 26(11) (2005) 1677-1681.
  • [21] Xu Q., Yang Z., Yin D., Zhang F., Catal. Commun. 9(1) (2008) 1579-1582.
  • [22] Kumar P., Kumar S., Husain K., Kumar A., Bioorg. Med. Chem. 18(14) (2010) 4965-4974.
  • [23] Zhang Z., Dong Y. W., Wang G. W., Chem. Lett. 32(10) (2003) 966-967.
  • [24] Thirunarayanan G., IUP. J. Chem. 3(4) (2010) 35-54.
  • [25] Thirunarayanan G., Elixir Org. Chem. 45 (2012) 7898-7905.
  • [26] Thirunarayanan G., Mayavel P., Thirumurthy K., Spectrochimica Acta. 91A (2012) 18-22.
  • [27] Sundararajan R., Arulkumaran R., Vijayakumar S., Kamalakkannan D., Suresh R., Ranganathan K., Sakthinathan S. P., Vanangamudi G., Thirumurthy K., Mayavel P., Thirunarayanan G., Int. J. Pharm. Chem. Sci. 1(4) (2012) 1657-1677.
  • [28] Janaki P., Sekar K. G., Thirunarayanan G., Org. Chem: An Indian J. 9(2) (2013) 68-80.
  • [29] Arulkumaran R., et al., International Letters of Chemistry, Physics and Astronomy 4 (2012) 17-38.
  • [30] Sundararajan R., Q-science Connect, 2013. DOI: http://dx.doi.org/10.5339/connect.2013.30
  • [31] Mitina V. G., Shenkoo A. O. D., Sukhorukov A. A., Lavrushin V. F., Teror. Eksp. Khim. 20(2) (1984) 147-150.
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  • [34] R. Arulkumaran, S. Vijayakumar, R. Sundararajan, S. P. Sakthinathan, D. Kamalakkannan, R. Suresh, K. Ranganathan, P. R. Rajakumar, G. Vanangamudi, G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 5 (2013) 21-38.
  • [35] S. P. Sakthinathan, R. Suresh, V. Mala, K.Sathiyamoorthi, D. Kamalakkannan, K. Ranganathan, R. Arulkumaran, S. Vijayakumar, R. Sundararajan, G. Vanangamudi, G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 6 (2013) 77-90.
  • [36] K. Sathiyamoorthi, V. Mala, R. Suresh, S. P. Sakthinathan, D. Kamalakkannan, K. Ranganathan, R. Arulkumaran, R. Sundararajan, S. Vijayakumar, G. Vanangamudi, G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 7(2) (2013) 102-119.
  • [37] G. Thirunarayanan, K. G. Sekar, International Letters of Chemistry, Physics and Astronomy 8(2) (2013) 160-174.
  • [38] K. G. Sekar, G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 8(3) (2013) 249-258.
  • [39] S. Vijayakumar, R. Arulkumaran, R. Sundararajan, S. P. Sakthinathan, R. Suresh, D. Kamalakkannan, K. Ranganathan, K. Sathiyamoorthy, V. Mala, G. Vanangamudi, G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 9(1) (2013) 68-86.
  • [40] G. Thirunarayanan, K. G. Sekar, International Letters of Chemistry, Physics and Astronomy 10(1) (2013) 18-34.
  • [41] R. Sundararajan, R. Arulkumaran, S. Vijayakumar, D. Kamalakkannan, R. Suresh, S. John Joseph, K. Ranganathan, S. P. Sakthinathan, G. Vanangamudi, G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 1 (2014) 67-73.
  • [42] S. John Joseph, R. Arulkumaran, D. Kamalakkannan, S. P. Sakthinathan, R. Sundararajan, R. Suresh, S. Vijayakumar, K. Ranganathan, N. Kalyanasundaram, G. Vanangamudi, G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 4 (2014) 48-65.
  • [43] G. Thirunarayanan, R. Sundararajan, R. Arulkumaran, International Letters of Chemistry, Physics and Astronomy 4 (2014) 82-97.
  • [44] G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 4 (2014) 109-116.
  • [45] G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 5 (2014) 89-98.
  • [46] S. John Joseph, D. Kamalakkannan, R. Arulkumaran, S. P. Sakthinathan, R. Suresh, R. Sundararajan, S. Vijayakumar, K. Ranganathan, G. Vanangamudi, G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 5 (2014) 99-123.
  • [47] G. Thirunarayanan, S. Pazhamalai, K. G. Sekar, International Letters of Chemistry, Physics and Astronomy 8 (2014) 38-46.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-f1bcfa04-921d-4b0c-9ed1-d01037979263
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