메뉴 건너뛰기




Volumn 67, Issue , 2013, Pages 14-18

Design, synthesis and insecticidal activities of novel acetamido derivatives containing N-pyridylpyrazole carboxamides

Author keywords

Acetamido derivatives; Insecticidal activity; N pyridylpyrazole carboxamides; Synthesis

Indexed keywords

ACETAMIDO DERIVATIVE; AMIDE; INSECTICIDE; N PYRIDYLPYRAZOLE CARBOXAMIDE; UNCLASSIFIED DRUG;

EID: 84880182138     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2013.06.023     Document Type: Article
Times cited : (37)

References (45)
  • 2
    • 33645050147 scopus 로고    scopus 로고
    • Microsatellites reveal a lack of structure in Australian populations of the diamondback moth, Plutella xylostella (L.)
    • N.M. Endersby, S.W. Mckechnie, P.M. Ridland, A.R. Weeks, Microsatellites reveal a lack of structure in Australian populations of the diamondback moth, Plutella xylostella (L.), Mol. Ecol. 15 (2006) 107-118.
    • (2006) Mol. Ecol. , vol.15 , pp. 107-118
    • Endersby, N.M.1    Mckechnie, S.W.2    Ridland, P.M.3    Weeks, A.R.4
  • 5
    • 33750313514 scopus 로고    scopus 로고
    • Genetics and evidence for an esterase-associated mechanism of resistance to indoxacarb in a field population of diamondback moth (Lepidoptera: Plutellidae)
    • DOI 10.1002/ps.1270
    • A.H. Sayye, D.J. Wright, Genetics and evidence for an esterase-associated mechanism of resistance to indoxacarb in a field population of diamondback moth (Lepidoptera: Plutellidae), Pest Manag. Sci. 62 (2006) 1045-1051. (Pubitemid 44620820)
    • (2006) Pest Management Science , vol.62 , Issue.11 , pp. 1045-1051
    • Sayyed, A.H.1    Wright, D.J.2
  • 6
    • 38349151219 scopus 로고    scopus 로고
    • Effects of insecticides on the fluidity of mitochondrial membranes of the diamondback moth, Plutella xylostella, resistant and susceptible to avermectin
    • J. Hu, P. Liang, X. Shi, X. Gao, Effects of insecticides on the fluidity of mitochondrial membranes of the diamondback moth, Plutella xylostella, resistant and susceptible to avermectin, J. Insect Sci. 8 (2008) 1-9.
    • (2008) J. Insect Sci. , vol.8 , pp. 1-9
    • Hu, J.1    Liang, P.2    Shi, X.3    Gao, X.4
  • 8
    • 67349227955 scopus 로고    scopus 로고
    • New and selective ryanodine receptor activators for insect control
    • G.P. Lahm, D. Cordova, J.D. Barry, New and selective ryanodine receptor activators for insect control, Bioorg. Med. Chem. 17 (2009) 4127-4133.
    • (2009) Bioorg. Med. Chem. , vol.17 , pp. 4127-4133
    • Lahm, G.P.1    Cordova, D.2    Barry, J.D.3
  • 9
    • 84864719177 scopus 로고    scopus 로고
    • Synthesis and insecticidal activities of novel anthranilic diamides containing acylthiourea and acylurea
    • J.F. Zhang, J.Y. Xu, B.L. Wang, Y.X. Li, L.X. Xiong, Y.Q. Li, Y. Ma, Z.M. Li, Synthesis and insecticidal activities of novel anthranilic diamides containing acylthiourea and acylurea, J. Agric. Food Chem. 60 (2012) 7565-7572.
    • (2012) J. Agric. Food Chem. , vol.60 , pp. 7565-7572
    • Zhang, J.F.1    Xu, J.Y.2    Wang, B.L.3    Li, Y.X.4    Xiong, L.X.5    Li, Y.Q.6    Ma, Y.7    Li, Z.M.8
  • 10
    • 78349249491 scopus 로고    scopus 로고
    • Design, synthesis and insecticidal evaluation of novel pyrazolecarboxamides containing cyano substituted N-pyridylpyrazole
    • Z.L. Liu, Q. Feng, L.X. Xiong, M.Z. Wang, Z.M. Li, Design, synthesis and insecticidal evaluation of novel pyrazolecarboxamides containing cyano substituted N-pyridylpyrazole, Chin. J. Chem. 28 (2010) 1757-1760.
    • (2010) Chin. J. Chem. , vol.28 , pp. 1757-1760
    • Liu, Z.L.1    Feng, Q.2    Xiong, L.X.3    Wang, M.Z.4    Li, Z.M.5
  • 11
    • 84865385477 scopus 로고    scopus 로고
    • Design, synthesis and biological activities of novel anthranilic diamide insecticide containing trifluoroethyl ether
    • Y. Zhao, Y.Q. Li, L.X. Xiong, H.X. Wang, Z.M. Li, Design, synthesis and biological activities of novel anthranilic diamide insecticide containing trifluoroethyl ether, Chin. J. Chem. 30 (2012) 1748-1758.
    • (2012) Chin. J. Chem. , vol.30 , pp. 1748-1758
    • Zhao, Y.1    Li, Y.Q.2    Xiong, L.X.3    Wang, H.X.4    Li, Z.M.5
  • 12
    • 84878064697 scopus 로고    scopus 로고
    • Synthesis, crystal structure and biological activity of novel anthranilic diamide insecticide containing alkyl ether group
    • Y. Zhao, L.P. Xu, J. Tong, Y.Q. Li, L.X. Xiong, F. Li, L.N. Peng, Z.M. Li, Synthesis, crystal structure and biological activity of novel anthranilic diamide insecticide containing alkyl ether group, Mol. Divers. 16 (2012) 711-725.
    • (2012) Mol. Divers. , vol.16 , pp. 711-725
    • Zhao, Y.1    Xu, L.P.2    Tong, J.3    Li, Y.Q.4    Xiong, L.X.5    Li, F.6    Peng, L.N.7    Li, Z.M.8
  • 14
    • 85030405894 scopus 로고    scopus 로고
    • Preparation of pyridinylpyrazole carbonylaminoindazole derivatives for use as insecticides
    • WO Patent 2009024341, 329797
    • O. Loiseleur, R.G. Hall, A.D. Stoller, G.W. Graig, A. Jeanguenat, A. Edmunds, Preparation of pyridinylpyrazole carbonylaminoindazole derivatives for use as insecticides, WO Patent 2009024341, Chem. Abstr., 150, 2009, 329797.
    • (2009) Chem. Abstr. , vol.150
    • Loiseleur, O.1    Hall, R.G.2    Stoller, A.D.3    Graig, G.W.4    Jeanguenat, A.5    Edmunds, A.6
  • 15
    • 84871111272 scopus 로고    scopus 로고
    • The story of a new insecticidal chemistry class: The diamides
    • A. Jeanguenat, The story of a new insecticidal chemistry class: the diamides, Pest Manag. Sci. 69 (2013) 7-14.
    • (2013) Pest Manag. Sci. , vol.69 , pp. 7-14
    • Jeanguenat, A.1
  • 17
    • 84870986652 scopus 로고    scopus 로고
    • Synthesis and insecticidal evaluation of novel N- pyridylpyrazolecarboxamides containing cyano substituent in the ortho-position
    • M.Z. Mao, Y.X. Li, Q.X. Liu, Y.Y. Zhou, X.L. Zhang, L.X. Xiong, Y.Q. Li, Z.M. Li, Synthesis and insecticidal evaluation of novel N- pyridylpyrazolecarboxamides containing cyano substituent in the ortho-position, Bioorg. Med. Chem. 23 (2013) 42-46.
    • (2013) Bioorg. Med. Chem. , vol.23 , pp. 42-46
    • Mao, M.Z.1    Li, Y.X.2    Liu, Q.X.3    Zhou, Y.Y.4    Zhang, X.L.5    Xiong, L.X.6    Li, Y.Q.7    Li, Z.M.8
  • 19
    • 67449147329 scopus 로고    scopus 로고
    • Synthesis, structure and biological activities of some novel anthranilic acid esters containing N-pyridylpyrazole
    • W.L. Dong, J.Y. Xu, L.X. Xiong, X.H. Liu, Z.M. Li, Synthesis, structure and biological activities of some novel anthranilic acid esters containing N-pyridylpyrazole, Chin. J. Chem. 27 (2009) 579-586.
    • (2009) Chin. J. Chem. , vol.27 , pp. 579-586
    • Dong, W.L.1    Xu, J.Y.2    Xiong, L.X.3    Liu, X.H.4    Li, Z.M.5
  • 20
    • 80052137366 scopus 로고    scopus 로고
    • Synthesis and insecticidal evaluation of novel N- pyridylpyrazolecarboxamides containing different substituents in the ortho-position
    • Q. Feng, G.P. Yu, L.X. Xiong, M.Z. Wang, Z.M. Li, Synthesis and insecticidal evaluation of novel N-pyridylpyrazolecarboxamides containing different substituents in the ortho-position, Chin. J. Chem. 29 (2011) 1651-1655.
    • (2011) Chin. J. Chem. , vol.29 , pp. 1651-1655
    • Feng, Q.1    Yu, G.P.2    Xiong, L.X.3    Wang, M.Z.4    Li, Z.M.5
  • 21
    • 82655181733 scopus 로고    scopus 로고
    • Synthesis and insecticidal activities of novel analogues of chlorantraniliprole containing nitro group
    • Q. Feng, M.Z. Wang, L.X. Xiong, Z.L. Liu, Z.M. Li, Synthesis and insecticidal activities of novel analogues of chlorantraniliprole containing nitro group, Chem. Res. Chin. Univ. 27 (2011) 610-613.
    • (2011) Chem. Res. Chin. Univ. , vol.27 , pp. 610-613
    • Feng, Q.1    Wang, M.Z.2    Xiong, L.X.3    Liu, Z.L.4    Li, Z.M.5
  • 23
    • 85030413376 scopus 로고    scopus 로고
    • N-cyanoalkyl anthranilamides as insecticides
    • WO Patent 2008064891, 10005
    • M. Muehlebach, G.W. Craig, N-cyanoalkyl anthranilamides as insecticides, WO Patent 2008064891, Chem. Abstr., 149, 2008, 10005.
    • (2008) Chem. Abstr. , vol.149
    • Muehlebach, M.1    Craig, G.W.2
  • 24
    • 85030404977 scopus 로고    scopus 로고
    • Preparation of anthranilamide derivative insecticides and acaricides
    • WO Patent 2007080131, 553327
    • M. Muehlebach, A. Jeanguenat, R.G. Hall, Preparation of anthranilamide derivative insecticides and acaricides, WO Patent 2007080131, Chem. Abstr., 147, 2007, 553327.
    • (2007) Chem. Abstr. , vol.147
    • Muehlebach, M.1    Jeanguenat, A.2    Hall, R.G.3
  • 25
    • 84859420549 scopus 로고    scopus 로고
    • Design, synthesis and insecticidal activities of novel pyrazole amides containing hydrazone substructures
    • J. Wu, B.A. Song, D.Y. Hu, M. Yue, S. Yang, Design, synthesis and insecticidal activities of novel pyrazole amides containing hydrazone substructures, Pest Manag. Sci. 68 (2012) 801-810.
    • (2012) Pest Manag. Sci. , vol.68 , pp. 801-810
    • Wu, J.1    Song, B.A.2    Hu, D.Y.3    Yue, M.4    Yang, S.5
  • 26
    • 85030413121 scopus 로고    scopus 로고
    • Pest controlling composition of an amide compound, a neonicotinoid and optionally other pesticides
    • WO Patent 2010098489, 327649
    • N. Sakamoto, S. Nishimura, Pest controlling composition of an amide compound, a neonicotinoid and optionally other pesticides, WO Patent 2010098489, Chem. Abstr., 153, 2010, 327649.
    • (2010) Chem. Abstr. , vol.153
    • Sakamoto, N.1    Nishimura, S.2
  • 27
    • 84859875586 scopus 로고    scopus 로고
    • Synthesis and insecticidal activity of novel N-pyridylpyrazole carbonyl thioureas
    • B.L. Wang, Y. Ma, L.X. Xiong, Z.M. Li, Synthesis and insecticidal activity of novel N-pyridylpyrazole carbonyl thioureas, Chin. J. Chem. 30 (2012) 815-821.
    • (2012) Chin. J. Chem. , vol.30 , pp. 815-821
    • Wang, B.L.1    Ma, Y.2    Xiong, L.X.3    Li, Z.M.4
  • 28
    • 84866352524 scopus 로고    scopus 로고
    • Synthesis of benzothiazole derivatives having acetamido and carbothioamido pharmacophore as anticonvulsant agents
    • M. Amir, S. Asif, I. Ali, M.Z. Hassan, Synthesis of benzothiazole derivatives having acetamido and carbothioamido pharmacophore as anticonvulsant agents, Med. Chem. Res. 21 (2012) 2661-2670.
    • (2012) Med. Chem. Res. , vol.21 , pp. 2661-2670
    • Amir, M.1    Asif, S.2    Ali, I.3    Hassan, M.Z.4
  • 29
    • 19544394603 scopus 로고    scopus 로고
    • Synthesis and antimicrobial activity of 4-phenyl/cyclohexyl-5-(1- phenoxyethyl)-3-[N- (2-thiazolyl)acetamido] thio-4H-1,2,4-triazole derivatives
    • G. Turan-Zitouni, Z.A. Kaplancikli, M.T. Yildiz, P. Chevallet, D. Kaya, Synthesis and antimicrobial activity of 4-phenyl/cyclohexyl-5-(1-phenoxyethyl)- 3-[N- (2-thiazolyl)acetamido] thio-4H-1,2,4-triazole derivatives, Eur. J. Med. Chem. 40 (2005) 607-613.
    • (2005) Eur. J. Med. Chem. , vol.40 , pp. 607-613
    • Turan-Zitouni, G.1    Kaplancikli, Z.A.2    Yildiz, M.T.3    Chevallet, P.4    Kaya, D.5
  • 31
    • 84856004741 scopus 로고    scopus 로고
    • Synthesis and cytotoxicity of O, O′ -dialkyl {[2-(substituted phenoxy)acetamido](substituted phenyl)methyl}phosphonates
    • L.H. Ning, W. Wang, Y.J. Liang, H. Peng, L.W. Fu, H.W. He, Synthesis and cytotoxicity of O, O′ -dialkyl {[2-(substituted phenoxy)acetamido] (substituted phenyl)methyl}phosphonates, Eur. J. Med. Chem. 48 (2012) 379-384.
    • (2012) Eur. J. Med. Chem. , vol.48 , pp. 379-384
    • Ning, L.H.1    Wang, W.2    Liang, Y.J.3    Peng, H.4    Fu, L.W.5    He, H.W.6
  • 33
    • 84982340225 scopus 로고
    • Synthesis and insecticidal activity of N-methylenefluoroacetamide derivatives
    • M. Pianka, D.J. Polton, Synthesis and insecticidal activity of N-methylenefluoroacetamide derivatives, J. Sci. Food Agri. 16 (1965) 330-341.
    • (1965) J. Sci. Food Agri. , vol.16 , pp. 330-341
    • Pianka, M.1    Polton, D.J.2
  • 34
    • 84884292112 scopus 로고
    • Fungicidal N-(2-cyano-2-alkoxyimino acetamido)cyclohexa-methyleneimine derivatives
    • US Patent 5310736, 114031
    • W. Lunkenheimer, W. Brandes, Fungicidal N-(2-cyano-2-alkoxyimino acetamido)cyclohexa-methyleneimine derivatives, US Patent 5310736, Chem. Abstr., 115, 1991, 114031.
    • (1991) Chem. Abstr. , vol.115
    • Lunkenheimer, W.1    Brandes, W.2
  • 35
    • 85030416605 scopus 로고    scopus 로고
    • Anthranilamide insecticides
    • WO Patent 2004033468, 339324
    • G.P. Lahm, T.P. Selby, T.M. Stevenson, Anthranilamide insecticides. WO Patent 2004033468, Chem. Abstr., 140, 2004, 339324.
    • (2004) Chem. Abstr. , vol.140
    • Lahm, G.P.1    Selby, T.P.2    Stevenson, T.M.3
  • 38
    • 84869991281 scopus 로고    scopus 로고
    • One-pot mechanosynthesis of aromatic amides and dipeptides from carboxylic acids and amines
    • V. Štrukil, B. Bartolec, T. Portada, I. Crossed D signilovic, I. Halasz, D. Margetic, One-pot mechanosynthesis of aromatic amides and dipeptides from carboxylic acids and amines, Chem. Commun. 48 (2012) 12100-12102.
    • (2012) Chem. Commun. , vol.48 , pp. 12100-12102
    • Štrukil, V.1    Bartolec, B.2    Portada, T.3    Dilovic, I.4    Halasz, I.5    Margetic, D.6
  • 39
    • 84874450375 scopus 로고    scopus 로고
    • Evaluation of alternative solvents in common amide coupling reactions: Replacement of dichloromethane and N, N-dimethylformamide
    • D.S. MacMillan, J. Murray, H.F. Sneddon, C. Jamieson, A.J.B. Watson, Evaluation of alternative solvents in common amide coupling reactions: replacement of dichloromethane and N, N-dimethylformamide, Green. Chem. 15 (2013) 596-600.
    • (2013) Green. Chem. , vol.15 , pp. 596-600
    • MacMillan, D.S.1    Murray, J.2    Sneddon, H.F.3    Jamieson, C.4    Watson, A.J.B.5
  • 40
    • 65349159817 scopus 로고    scopus 로고
    • Synthesis and structure-activity relationships of substituted cinnamic acids and amide analogues: A new class of herbicides
    • S. Vishnoi, V. Agrawal, V.K. Kasana, Synthesis and structure-activity relationships of substituted cinnamic acids and amide analogues: a new class of herbicides, J. Agric. Food Chem. 57 (2009) 3261-3265.
    • (2009) J. Agric. Food Chem. , vol.57 , pp. 3261-3265
    • Vishnoi, S.1    Agrawal, V.2    Kasana, V.K.3
  • 41
    • 78649686293 scopus 로고    scopus 로고
    • Synthesis and insecticidal activities of novel anthranilic diamides containing modified N-pyridyl pyrazoles
    • Q. Feng, Z.L. Liu, L.X. Xiong, M.Z. Wang, Y.Q. Li, Z.M. Li, Synthesis and insecticidal activities of novel anthranilic diamides containing modified N-pyridyl pyrazoles, J. Agric. Food Chem. 58 (2010) 12327-12336.
    • (2010) J. Agric. Food Chem. , vol.58 , pp. 12327-12336
    • Feng, Q.1    Liu, Z.L.2    Xiong, L.X.3    Wang, M.Z.4    Li, Y.Q.5    Li, Z.M.6
  • 42
    • 78049300160 scopus 로고    scopus 로고
    • Synthesis, insecticidal activity, and structure-activity relationship of trifluoromethyl-containing phthalic acid diamide structures
    • M.L. Feng, Y.F. Li, H.J. Zhu, L. Zhao, B.B. Xi, J.P. Ni, Synthesis, insecticidal activity, and structure-activity relationship of trifluoromethyl-containing phthalic acid diamide structures, J. Agric. Food Chem. 58 (2010) 10999-11006.
    • (2010) J. Agric. Food Chem. , vol.58 , pp. 10999-11006
    • Feng, M.L.1    Li, Y.F.2    Zhu, H.J.3    Zhao, L.4    Xi, B.B.5    Ni, J.P.6
  • 43
    • 0000722909 scopus 로고
    • A method of computing the effectiveness of an insecticide
    • W.S. Abbott, A method of computing the effectiveness of an insecticide, J. Econ. Entomol. 18 (1925) 265-267.
    • (1925) J. Econ. Entomol. , vol.18 , pp. 265-267
    • Abbott, W.S.1
  • 44
    • 57849150543 scopus 로고    scopus 로고
    • Toxicities of novel insecticide chlorfenpyr against several insects in lab
    • Y.J. Wang, X.M. Ou, H. Pei, X.M. Lin, K. Yu, Toxicities of novel insecticide chlorfenpyr against several insects in lab, Agrochem. Res. Appl. 10 (2006) 20-23.
    • (2006) Agrochem. Res. Appl. , vol.10 , pp. 20-23
    • Wang, Y.J.1    Ou, X.M.2    Pei, H.3    Lin, X.M.4    Yu, K.5
  • 45
    • 84865448911 scopus 로고    scopus 로고
    • 5-Chloro-6-phenyl-N-substitutied pyridazin-3(2H) -one: Synthesis, insecticidal activity against Plutella xylostella (Linnaeus) and their SAR study
    • J. Wu, S.H. Kang, Q.K. Yuan, L.J. Luo, J. Ma, Q.C. Shi, S. Yang, 5-Chloro-6-phenyl-N-substitutied pyridazin-3(2H) -one: synthesis, insecticidal activity against Plutella xylostella (Linnaeus) and their SAR study, Molecules 17 (2012) 9413-9420.
    • (2012) Molecules , vol.17 , pp. 9413-9420
    • Wu, J.1    Kang, S.H.2    Yuan, Q.K.3    Luo, L.J.4    Ma, J.5    Shi, Q.C.6    Yang, S.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.