PL EN


Preferences help
enabled [disable] Abstract
Number of results
2016 | 71 | 2 |
Article title

Synthesis, spectral studies and insect antifeedant activities of some 4-substituted 1-naphthacyl bromide and its esters

Content
Title variants
Languages of publication
EN
Abstracts
EN
About nine 4-substituted 1-naphthacyl bromides and its esters have been synthesized by greener synthetic method using fly-ash catalyzed water mediated reaction.  These acyl bromides and esters have been characterized by their physical constants, Mass, IR and NMR spectral data.  These carbonyl frequencies(cm-1) of existed rotomers of these compounds have been assigned and correlated with Hammett substituent constants, F, R and Swain-Lupton’s parameters.  The insect antifeedant activities of the synthesized acyl bromide and esters have been evaluated using 4th instar larvae Achoea Janatha L.
Year
Volume
71
Issue
2
Physical description
Dates
published
2016
online
03 - 04 - 2017
Contributors
References
  • G. Goel, H. P. S. Makkar, G. Francis, K. Becker, Int. J. Toxicol., 26, 279, (2007).
  • G. Thirunarayanan, P. Mayavel, K. Thirumurthy, Spectrochim. Acta., 91A, 18, (2012).
  • G. Thirunarayanan, G. Vanangamudi, Arkivoc., 12, 58, (2006).
  • S. Kajigaeshi, T. Kakinami, T. Okamoto, S. Fujisaki, Bull. Chem. Soc. Jpn., 60, 1159, (1987).
  • U. Bora, D. Dey, S. Dhar, M. K. Chaudhuri, Pure Appl. Chem., 73, 93, (2001).
  • M. K. Chaudhuri, A. T. Khan, B. K. Patel, D. Dey, W. Kharmawphlang, T. R. Lakshmiprapha, G. C. Mandal, Tetrahedron Lett. 39, 8163, (1998).
  • H. Zhao, Z. Song, J. V. Cowins, O. Olubajo, Int. J. Mol. Sci., 9, 33, (2008).
  • C. T. Chen, Y. S. Munot, J. Org. Chem., 70, 8625, (2005).
  • J. D. Lou, Z. N. Xu, Tetrahedron Lett., 43, 6149,(2002).
  • B. Kalluraya, G. Ray, Indian J. Chem., 42(B), 2556, (2003).
  • G. Thirunarayanan, M. Gopalakrishnan, G. Vanangamudi, Spectrochim. Acta. 67A, 1106, (2007).
  • F. F. Bamoharram, M. M. Heravi, M. Roshani, M. Jahangir, A. Gharib, J. Mol. Catal., 271A, 126, (2007).
  • S. Adimurthy, G. Ramachandraiah, A.V. Bedekar, S. Ghosh, B. C. Ranu, P. K. Gosh, Green Chem., 8, 916,(2006).
  • H. Sharghi, M. Hosseini Sarvari, Tetrahedron., 59, 3627, (2003).
  • B. D. Paul, C. Dreka, J. L. Summers, M. L. Smith, J. Anal. Toxicol., 20, 506, (1996).
  • J. Deli, T. Loand, D. Szabo, A. Foldsi, Pharmazie., 39, 539, (1984).
  • L.Sun, S. Zheng, J. Wang, X. Shen, Indian J. Chem., 41B, 1319, (2002).
  • M. G. Ahmed, S. A. Ahmed, U. K. R. Romman, T. Sultana, M. A. Hena, S. Kiyooka, Indian J. Chem., 41B, 368, (2002).
  • L. Q. Wu, C. G. Yang, Y. F. Wu, L. M. Yang, J. Chin. Chem. Soc., 56, 606, (2009).
  • L. C. King, G. K. Ostrum, J. Org. Chem., 29, 3459, (1964).
  • P. A. Levene, Org. Synth., II, 88, (1943).
  • L. A. Yanovskaya, P. A., Terentev, L. N. Belenkii, J. Gen. Chem., 22, 1594, (1952).
  • F. Krohnke, K. Ellegast, Chem. Ber., 86, 1556 (1953).
  • E. I. Sanches, M. J. Fumarola, J. Org. Chem., 47,1588, (1982).
  • A. N. Mayeno, A. J. Curran, R. L. Roberts, C. S. Foote, J. Biol. Chem., 264, 5660 (1989).
  • D. I. Cajetan, T. Bekele, S. France, J. Wolfer, A. Weatherwax, A. E. Taggi, T. Lectka, J. Org. Chem., 71, 8946, (2006).
  • R. E. Lovins, L. J. Anrews, R. W. Keef, J. Org. Chem., 28, 2847, (1963).
  • N. E. Starostenko, N. O. Adeeva, F. N. Zeiberlikh, L. N. Kurkovskaya, N. N. Suvorov, Chem. Heterocycl. Compd., 23, 271, (1987).
  • S. B. Patwari, M. A. Baseer, Y. B. Vibhute, S. R. Bhusare, Tetrhedron Lett., 44, 4893, (2003).
  • K. Wakasugi, A. Nakamura, Y. Tanabe, Tetrahedron Lett., 42, 7427, (2001).
  • D. Taber, J. Am. Chem. Soc., 128, 13052, (2006).
  • W. J. Yoo, C. J. Li, J. Org. Chem., 71, 6266, (2006).
  • R. V. H. Jones, W. E. Lindsell, D. D. Palmer, P. N. Preston, A. J. Whitton, Tetrahedron Lett., 46, 8695, (2005).
  • M. Pittelkow, F.S. Kamounah, U. Boas, B. Pedersen, J. B. Christensen, Synthesis., 2485, (2004)
  • H. Merima, W. Gunnar, Cellulose., 14, 347, (2007).
  • Y. Halpern, US Patent No. 5035840, (1991).
  • R. Moumne, S. Lavielle, P. Karoyan, J. Org. Chem., 71, 3332, (2006).
  • W.W.Christie, Advances in Lipid Methodology II,(Oily Press, Dundee),(1993), pp.69-111.
  • P. Ananthakrishna Nadar, C. Gnanasekaran, Indian J. Chem., 14B, 606, (1976).
  • G. Thirunarayanan, G. Vanangamudi, V. Sathiyendiran, K. Ravi, Indian J. Chem., 50B, 593, (2011).
  • M. Gopalakrishnan, P. Sureshkumar, V. Kanagarajan, J. Thanusu, Catal. Commun., 6, 753, (2005).
  • M. Gopalakrishnan, P. Sureshkumar, V. Kanagarajan, J. Thanusu, R. Govindaraju, Arkivoc., 13, 130, (2006).
  • M. Gopalakrishnan, P. Sureshkumar, V. Kanagarajan, J. Korean Chem. Soc., 51(6), 520, (2007).
  • A. Perjessy, M. Lacucova, Coll. Czech. Chem. Commun., 36, 2944, (1971).
  • C. M. Devia, N. B. Pappano, N. B. Debasttista, Rev. Microbiol., 29, 307, (1998).
  • V. Krishnakumar, R. Ramasamy, Indian J. Pure Appl. Phys., 40, 252, (2002).
  • A. Sharma, V. P. Gupta, A. Virdi, Indian J. Pure and App. Phys., 40, 246, (2002).
  • G. K. Dass, Indian J. Chem., 23A, 23, (2001).
  • P. R. Griffiths, J. M. Chalmers, (2003), Handbook of Vibrational Spectroscopy, (John Wiley & Sons Inc., Chinchester, vol.4, pp.2756.
  • C. Pellerin, I. Pelletier, Lab International Plus., 19, 10, (2005).
  • E. T. McBee, D. L. Christman, J. Am. Chem. Soc., 77, 755, (1955).
  • R. S. Rasmussen, R. R. Brattain, J. Am. Chem. Soc., 71, 1073, (1949).
  • M. Hauptdchein, C. S. Stokes, E. A. Nodiff, J. Am. Chem. Soc., 74, 4005, (1952).
  • L. J. Bellamy, R. L. Williams, J. Chem. Soc., 4297, (1957).
  • J. Shorter, (1973). Correlation analysis in Chemistry: An introduction to linear free energy relationships, Clarendon Press, London.
  • C. G. Swain, E. C. Lupton, Jr., J. Am. Chem. Soc., 90, 4328, (1968).
  • M. Mišić-Vuković, M. Radojković-Veličković, J. Serb. Chem. Soc. Rev., 63, 585, (1998)
  • S. Jovanovic, D. Mijin, M. M. Vuković, Arkivoc., 10, 116, (2006).
  • P. Ananthakrishna Nadar, C. Gnanasekaran, Indian J. Chem., 17B, 391, (1979).
  • S. R. Annapoorna, M. Prasad Rao, B. Sethuram, Indian J. Chem., 41A, 1341,(2002).
  • G. Thirunarayanan, P. Ananthakrishna Nadar, J. Indian Chem. Soc., 83, 1107 (2006).
  • G. Thirunarayanan, P. Ananthakrishna Nadar, J. Korean Chem. Soc., 50, 183, (2006).
  • R. Suresh, D. Kamalakkannan, D. Ranganathan, R. Arulkumaran, S.P. Sakthinathan, S. Vijayakumar, K. Sathiyamoorthi, V. Mala, G. Vanangamudi, K. Thirumurthy, P. Mayavel, G. Thirunarayanan, Spectrochim. Acta. 101A, 239, (2013).
  • G. Thirunarayanan, Indian J. Chem., 46B, 1511, (2007).
  • P. Janaki, K. G. Sekar, G. Thirunarayanan, J. Saudi Chem. Soc., 20, 58, (2016).
  • M. C. Unlusoy, N. Altanlar, R. Ertan, Turk. J. Chem., 29, 187, (2005).
  • B. Ahilstrom, M. C. Bertillson, R. A. Thompson, Antimicrob. Agents Chemother., 39, 50, (1995).
  • A. A. Williams, E. W. Sugandhi, R. V. Macri, J. O. Falkinham, R. D. Gandour, J. Antimicrob. Chemother., 59, 451, (2007).
  • O. E. Nwfor, M. J. Ikenebomeh, African J. Biotechnol., 8, 2843, (2009).
  • W. B. Wan, J. R. Beadle, C. Hartline, E. R., Kern, S. L. Ciesla, N. Valiaeva, K. Y. Hostetler, Antimicrob Agents Chemother., 49, 656, (2005).
  • B. C. Brasileiro, V. R. Pizziolo, D. S. Raslan, C. M. Jamal, D. Silveira, Brazilian J. Pharm. Sci., 42, 195, (2006).
  • A. Konopka, T. Zakharova, M. Bischoff, L. Oliver, C. Nakatsu, R. F. Turco, Appl. Environ. Micorbiol., 65, 3356, (1999).
  • S. Y. Liu, F. Sporer, M. Wink, J. Jourdane, R. Henning, Y. L. Li, A. Ruppel, Trop. Med. Int. Health., 2179, (1997).
  • G. Thirunarayanan, J. Indian Chem. Soc., 85, 447, (2008).
  • G. Thirunarayanan, S. Surya, S. Srinivasan, G. Vanangamudi, V. Sathiyendiran, Spectrochim. Acta., 75A, 152, (2010).
  • V. G. Dethler, (1947). Chemical insect attractants and repellants, Philadeciphia, p. 210.
Document Type
Publication order reference
Identifiers
YADDA identifier
bwmeta1.element.ojs-doi-10_17951_aa_2016_71_2_67
JavaScript is turned off in your web browser. Turn it on to take full advantage of this site, then refresh the page.