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Insect antifeedant potent halogen substituted phenyl chalcones

Treść / Zawartość
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Some 2′,3′,4′-trichlorophenyl chalcones [(E)-1-(2,3,4-trichlorophenyl)-3-(substituted phenyl)-2-propen-1-ones] have been synthesised using sulfated Titania catalyzed solvent-free aldol condensation between 2,3,4-trichloroacetophenone and substituted benzaldehydes. The purities of synthesised chalcones were checked by their analytical, physical and spectroscopic data reported in literature. The insect antifeedant activities of these chalcones have been studied using 4th instar larvae Achoea Janata L by castor leaf disc bio-assay method. The chloro substituted chalcones shows significant insect antifeedant activity.
Rocznik
Tom
Strony
67--73
Opis fizyczny
Bibliogr. 41 poz., rys., tab., wz.
Twórcy
  • PG & Research Department of Chemistry, Government Arts College, C-Mutlur, Chidambaram - 608102, India.
  • PG & Research Department of Chemistry, Government Arts College, C-Mutlur, Chidambaram - 608102, India.
  • PG & Research Department of Chemistry, Government Arts College, C-Mutlur, Chidambaram - 608102, India.
  • PG & Research Department of Chemistry, Government Arts College, C-Mutlur, Chidambaram - 608102, India.
autor
  • PG & Research Department of Chemistry, Government Arts College, C-Mutlur, Chidambaram - 608102, India.
autor
  • PG & Research Department of Chemistry, Government Arts College, C-Mutlur, Chidambaram - 608102, India.
  • PG & Research Department of Chemistry, Government Arts College, C-Mutlur, Chidambaram - 608102, India.
  • PG & Research Department of Chemistry, Government Arts College, C-Mutlur, Chidambaram - 608102, India.
  • PG & Research Department of Chemistry, Government Arts College, C-Mutlur, Chidambaram - 608102, India.
  • Department of Chemistry, Annamalai University, Annamalainagar - 608002, Inida.
Bibliografia
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  • [30] Thirunarayanan G., Thirumurthy K., Vanangamudi G., Subramanian M., Arulkumaran R., Kamalakkannan D. et al. Elixir Org Chem. 45 (2012) 7898-7905.
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  • [34] Sundararajan R., Arulkumaran R., Vijayakumar S., Kamalakkannan D., Suresh R., John Joseph S., Ranganathan K., Vanangamudi G., Subramanian M., Thirunarayanan G., Muthuvel I., Krishnakumar B., Q-Science Connect. 2013. DOI: http://dx.doi.org/10.5339/connect.2013.30
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  • [38] K. Ranganathan, R. Suresh, D. Kamalakkannan, R. Arulkumaran, R. Sundararajan, S. P. Sakthinathan, S. Vijayakumar, G. Vanangamudi, K. Thirumurthy, P. Mayavel, G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 4 (2012) 66-75.
  • [39] 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.
  • [40] 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.
  • [41] Thirunarayanan G., Sekar K. G., International Letters of Chemistry, Physics and Astronomy 10 (2013) 18-34.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-05cbecb7-7b86-4901-905b-b08e65574bc5
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