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Volumn 62, Issue 46, 2014, Pages 11054-11061

Insecticidal activities of chiral N -trifluoroacetyl sulfilimines as potential ryanodine receptor modulators

Author keywords

insecticidal activity; optically active; sulfiliminyl

Indexed keywords

FUNCTIONAL GROUPS; SCAFFOLDS; STEREOCHEMISTRY; X RAY DIFFRACTION ANALYSIS;

EID: 84914127481     PISSN: 00218561     EISSN: 15205118     Source Type: Journal    
DOI: 10.1021/jf503513n     Document Type: Article
Times cited : (35)

References (44)
  • 4
    • 84865245638 scopus 로고    scopus 로고
    • Insecticides affecting calcium homeostasis - Flubendiamide
    • 2 nd ed. Kramer, W. Schirmer, U. Jeschke, P. Witschel, M. Wiley-VCH Verlag: Weinheim, Germany, Vol. 3
    • Hamaguchi, H.; Hirooka, T. Insecticides affecting calcium homeostasis-flubendiamide. In Modern Crop Protection Compounds, 2 nd ed.; Kramer, W.; Schirmer, U.; Jeschke, P.; Witschel, M., Eds.; Wiley-VCH Verlag: Weinheim, Germany, 2012; Vol. 3, pp 1396-1409.
    • (2012) Modern Crop Protection Compounds , pp. 1396-1409
    • Hamaguchi, H.1    Hirooka, T.2
  • 15
    • 67349227955 scopus 로고    scopus 로고
    • New and selective ryanodinereceptor activators for insect control
    • Lahm, G. P.; Cordova, D.; Barry, J. D. New and selective ryanodinereceptor activators for insect control Bioorg. Med. Chem. 2009, 17, 4127-4133
    • (2009) Bioorg. Med. Chem. , vol.17 , pp. 4127-4133
    • Lahm, G.P.1    Cordova, D.2    Barry, J.D.3
  • 18
    • 84914172336 scopus 로고    scopus 로고
    • DuPont Rynaxypyr Insect Control Technical Bulletin.
    • DuPont Rynaxypyr Insect Control Technical Bulletin; http://www2.dupont.com/Production-Agriculture/en-US/assets/downloads/pdfs/Rynaxypyr-Tech-Bulletin.pdf.
  • 19
    • 84903976366 scopus 로고    scopus 로고
    • Chiral dicarboxamide scaffolds containing sulfiliminyl moiety as potential ryanodine receptor activators
    • Zhou, S.; Jia, Z. H.; Xiong, L. X.; Yan, T.; Yang, N.; Wu, G. P.; Song, H. B.; Li, Z. M. Chiral dicarboxamide scaffolds containing sulfiliminyl moiety as potential ryanodine receptor activators J. Agric. Food Chem. 2014, 62 (27) 6269-6277
    • (2014) J. Agric. Food Chem. , vol.62 , Issue.27 , pp. 6269-6277
    • Zhou, S.1    Jia, Z.H.2    Xiong, L.X.3    Yan, T.4    Yang, N.5    Wu, G.P.6    Song, H.B.7    Li, Z.M.8
  • 21
    • 34848848499 scopus 로고    scopus 로고
    • Fluorine in pharmaceuticals: Looking beyond intuition
    • Muller, K.; Faeh, C.; Diederich, F. Fluorine in pharmaceuticals: looking beyond intuition Science 2007, 317, 1881-1887
    • (2007) Science , vol.317 , pp. 1881-1887
    • Muller, K.1    Faeh, C.2    Diederich, F.3
  • 22
    • 81755183006 scopus 로고    scopus 로고
    • Traceless solide-phase synthesis of trifluoromethylarenes
    • Dobele, M.; Wiehn, M. S.; Brase, S. Traceless solide-phase synthesis of trifluoromethylarenes Angew. Chem., Int. Ed. 2011, 50, 11533-11535
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 11533-11535
    • Dobele, M.1    Wiehn, M.S.2    Brase, S.3
  • 23
    • 0034703491 scopus 로고    scopus 로고
    • Nucleophili trifluoromethylation reactions of organic compounds with (trifluoromethyl) trimethylsilane
    • Singh, R. P.; Shreeve, J. M. Nucleophili trifluoromethylation reactions of organic compounds with (trifluoromethyl) trimethylsilane Tetrahedron 2000, 56, 7613-7632
    • (2000) Tetrahedron , vol.56 , pp. 7613-7632
    • Singh, R.P.1    Shreeve, J.M.2
  • 24
    • 77955577649 scopus 로고    scopus 로고
    • Electrophilic trifluoromethylation of arenes and N-heteroarenes using hypervalent iodine reagents
    • Wiehn, M. S.; Vinogradova, E. V.; Togni, A. Electrophilic trifluoromethylation of arenes and N-heteroarenes using hypervalent iodine reagents J. Fluorine Chem. 2010, 131, 951-957
    • (2010) J. Fluorine Chem. , vol.131 , pp. 951-957
    • Wiehn, M.S.1    Vinogradova, E.V.2    Togni, A.3
  • 25
    • 77949279157 scopus 로고    scopus 로고
    • Reactivity of a hypervalent iodine trifluoromethylation reagent toward THF: Ring opening and formation of trifluoromethyl ethers
    • Fantasia, S.; Welch, J. M.; Togni, A. Reactivity of a hypervalent iodine trifluoromethylation reagent toward THF: ring opening and formation of trifluoromethyl ethers J. Org. Chem. 2010, 75, 1779-1782
    • (2010) J. Org. Chem. , vol.75 , pp. 1779-1782
    • Fantasia, S.1    Welch, J.M.2    Togni, A.3
  • 26
    • 84904260110 scopus 로고    scopus 로고
    • Design, synthesis, structure-activity relationship and insecticidal activities of trifluoromethyl-containing sulfiliminyl and sulfoximinyl phthalic acid diamide structures
    • Zhou, S.; Yan, Tao.; Wang, B. L.; Li, Z. Design, synthesis, structure-activity relationship and insecticidal activities of trifluoromethyl-containing sulfiliminyl and sulfoximinyl phthalic acid diamide structures Chin. J. Chem. 2014, 32 (7) 567-562
    • (2014) Chin. J. Chem. , vol.32 , Issue.7 , pp. 567-562
    • Zhou, S.1    Yan, T.2    Wang, B.L.3    Li, Z.4
  • 27
    • 34848854176 scopus 로고    scopus 로고
    • Iodine and metal-free synthesis of N -cyano sulfilimines: Novel and easy access of NH-sulfoximines
    • Garcia Mancheno, O.; Bistri, O.; Bolm, C. Iodine and metal-free synthesis of N -cyano sulfilimines: novel and easy access of NH-sulfoximines Org. Lett. 2007, 19, 3809-3811
    • (2007) Org. Lett. , vol.19 , pp. 3809-3811
    • Garcia Mancheno, O.1    Bistri, O.2    Bolm, C.3
  • 29
    • 0000722909 scopus 로고
    • A method of computing the effectiveness of an insecticide
    • Abbott, W. S. A method of computing the effectiveness of an insecticide J. Econ. Entomol. 1925, 18, 265-267
    • (1925) J. Econ. Entomol. , vol.18 , pp. 265-267
    • Abbott, W.S.1
  • 30
    • 0000604401 scopus 로고
    • Presentation dun programme Basicdanalyse log-probit pour miero-ordinateur
    • Raymond, M. Presentation dun programme Basicdanalyse log-probit pour miero-ordinateur Cah. ORSTOM Ser. Ent. Med. Parasitol. 1985, 23, 117-121
    • (1985) Cah. ORSTOM Ser. Ent. Med. Parasitol. , vol.23 , pp. 117-121
    • Raymond, M.1
  • 31
    • 64549094865 scopus 로고    scopus 로고
    • Evaluation of two resistance monitoring methods in Helicoverpa armigera: Topical application method and leaf dipping method
    • Wu, Y. D.; Shen, J. L.; Chen, J.; Lin, X. W.; Li, A. M. Evaluation of two resistance monitoring methods in Helicoverpa armigera: topical application method and leaf dipping method Plant Prot. 1996, 22 (5) 3-6
    • (1996) Plant Prot. , vol.22 , Issue.5 , pp. 3-6
    • Wu, Y.D.1    Shen, J.L.2    Chen, J.3    Lin, X.W.4    Li, A.M.5
  • 32
    • 36749026740 scopus 로고    scopus 로고
    • The toxicity testing of five insecticides to different instar larvae of Spodoptera exigua
    • Ma, H.; Wang, K. Y.; Xia, X. M.; Zhang, Y.; Guo, Q. L. The toxicity testing of five insecticides to different instar larvae of Spodoptera exigua Mod. Agrochem. 2006, 5, 44-46
    • (2006) Mod. Agrochem. , vol.5 , pp. 44-46
    • Ma, H.1    Wang, K.Y.2    Xia, X.M.3    Zhang, Y.4    Guo, Q.L.5
  • 33
    • 12644293853 scopus 로고
    • Recommended methods for measurement of pest resistance to pesticides
    • FAO: Rome, Italy, pp and 119 - 122.
    • Busivine, J. R. Recommended methods for measurement of pest resistance to pesticides. FAO Plant Production and Protection Paper 21; FAO: Rome, Italy, 1980; pp 3-13 and 119-122.
    • (1980) FAO Plant Production and Protection Paper 21 , pp. 3-13
    • Busivine, J.R.1
  • 34
    • 84878341984 scopus 로고    scopus 로고
    • An unexpected product N -(3-((2-fluorobenzyl)thio)-5-methyl-4 H -1,2,4-triazol-4-yl)acetimidamide: Synthesis and structure analysis
    • Sun, N. B.; Liu, X. H.; Weng, J. Q.; Tan, C. X. An unexpected product N -(3-((2-fluorobenzyl)thio)-5-methyl-4 H -1,2,4-triazol-4-yl)acetimidamide: synthesis and structure analysis J. Chem. Soc. Pak. 2013, 35, 499-502
    • (2013) J. Chem. Soc. Pak. , vol.35 , pp. 499-502
    • Sun, N.B.1    Liu, X.H.2    Weng, J.Q.3    Tan, C.X.4
  • 35
    • 84888884330 scopus 로고    scopus 로고
    • Synthesis, crystal structure, and theoretical studies of N -(4-((4-chlorobenzyl)oxy)phenyl)-4-(trifluoromethyl)pyrimidin-2-amine
    • Jin, J. C.; Sun, Z. H.; Yang, M. Y.; Wu, J.; Liu, X. H. Synthesis, crystal structure, and theoretical studies of N -(4-((4-chlorobenzyl)oxy)phenyl)-4-(trifluoromethyl)pyrimidin-2-amine J. Chem. 2013, 2013 521757
    • (2013) J. Chem. , vol.2013 , pp. 521757
    • Jin, J.C.1    Sun, Z.H.2    Yang, M.Y.3    Wu, J.4    Liu, X.H.5
  • 36
    • 84872803011 scopus 로고    scopus 로고
    • Synthesis, crystal structure, and fungicidal activity of 5-(4-cyclopropyl-5-((3-fluorobenzyl)thio)-4 H -1,2,4-triazol-3-yl)-4-methyl-1,2,3-thiadiazole
    • Liu, X. H.; Weng, J. Q.; Tan, C. X. Synthesis, crystal structure, and fungicidal activity of 5-(4-cyclopropyl-5-((3-fluorobenzyl)thio)-4 H -1,2,4-triazol-3-yl)-4-methyl-1,2,3-thiadiazole J. Chem. 2013, 2013 306361
    • (2013) J. Chem. , vol.2013 , pp. 306361
    • Liu, X.H.1    Weng, J.Q.2    Tan, C.X.3
  • 37
    • 84863011823 scopus 로고    scopus 로고
    • (E)-(4-Bromobenzylidene)amino cyclopropanecarboxylate
    • Liu, X. H.; Tan, C. X.; Weng, J. Q.; Liu, H. J. (E)-(4-Bromobenzylidene)amino cyclopropanecarboxylate Acta Crystallogr. E 2012, 68, O493
    • (2012) Acta Crystallogr. e , vol.68 , pp. 493
    • Liu, X.H.1    Tan, C.X.2    Weng, J.Q.3    Liu, H.J.4
  • 38
    • 84862169309 scopus 로고    scopus 로고
    • Synthesis, crystal structure, and fungicidal activity of a novel 1,2,3-thiadiazole compound
    • Tan, C. X.; Weng, J. Q.; Liu, Z. X.; Liu, X. H.; Zhao, W. G. Synthesis, crystal structure, and fungicidal activity of a novel 1,2,3-thiadiazole compound Phosphorus Sulfur Silicon Relat. Elem. 2012, 187, 990-996
    • (2012) Phosphorus Sulfur Silicon Relat. Elem. , vol.187 , pp. 990-996
    • Tan, C.X.1    Weng, J.Q.2    Liu, Z.X.3    Liu, X.H.4    Zhao, W.G.5
  • 39
    • 84905757846 scopus 로고    scopus 로고
    • Novel phthalamides containing sulfiliminyl moieties and derivatives as potential ryanodine receptor modulators
    • Zhou, S.; Yan, T.; Li, Y. X.; Jia, Z. H.; Wang, B. L.; Zhao, Y.; Qiao, Y. Y.; Xiong, L. X.; Li, Y. Q.; Li, Z. M. Novel phthalamides containing sulfiliminyl moieties and derivatives as potential ryanodine receptor modulators Org. Biomol Chem. 2014, 12 (34) 6643-6652
    • (2014) Org. Biomol Chem. , vol.12 , Issue.34 , pp. 6643-6652
    • Zhou, S.1    Yan, T.2    Li, Y.X.3    Jia, Z.H.4    Wang, B.L.5    Zhao, Y.6    Qiao, Y.Y.7    Xiong, L.X.8    Li, Y.Q.9    Li, Z.M.10
  • 40
    • 84905815057 scopus 로고    scopus 로고
    • Microwave assistant one pot synthesis, crystal structure, antifungal activities and 3D-QSAR of novel 1,2,4-triazolo[4,3-9 a ]pyridines
    • Liu, X. H.; Sun, Z. H.; Yang, M. Y.; Tan, C. X.; Weng, J. Q.; Zhang, Y. G.; Ma, Y. Microwave assistant one pot synthesis, crystal structure, antifungal activities and 3D-QSAR of novel 1,2,4-triazolo[4,3-9 a ]pyridines Chem. Biol. Drug Des. 2014, 84, 342-347
    • (2014) Chem. Biol. Drug Des. , vol.84 , pp. 342-347
    • Liu, X.H.1    Sun, Z.H.2    Yang, M.Y.3    Tan, C.X.4    Weng, J.Q.5    Zhang, Y.G.6    Ma, Y.7
  • 41
    • 84890924210 scopus 로고    scopus 로고
    • Design, synthesis, biological activities and 3D-QSAR of new N, N diacylhydrazines containing 2,4-dichlorophenoxy moieties
    • Sun, G. X.; Sun, Z. H.; Yang, M. Y.; Liu, X. H.; Ma, Y.; Wei, Y. Y. Design, synthesis, biological activities and 3D-QSAR of new N, N diacylhydrazines containing 2,4-dichlorophenoxy moieties Molecules 2013, 18, 14876-14891
    • (2013) Molecules , vol.18 , pp. 14876-14891
    • Sun, G.X.1    Sun, Z.H.2    Yang, M.Y.3    Liu, X.H.4    Ma, Y.5    Wei, Y.Y.6
  • 42
    • 84887150634 scopus 로고    scopus 로고
    • Design, synthesis, antifungal activities and 3D-QSAR of new N, N diacylhydrazines containing 2,4-dichlorophenoxy moiety
    • Sun, N. B.; Shi, Y. X.; Liu, X. H.; Ma, Y.; Tan, C. X.; Weng, J. Q.; Jin, J. Z.; Li, B. J. Design, synthesis, antifungal activities and 3D-QSAR of new N, N diacylhydrazines containing 2,4-dichlorophenoxy moiety Int. J. Mol. Sci. 2013, 14, 21741-21756
    • (2013) Int. J. Mol. Sci. , vol.14 , pp. 21741-21756
    • Sun, N.B.1    Shi, Y.X.2    Liu, X.H.3    Ma, Y.4    Tan, C.X.5    Weng, J.Q.6    Jin, J.Z.7    Li, B.J.8
  • 43
    • 84923263557 scopus 로고    scopus 로고
    • Synthesis, crystal structure, herbicidal activities and 3D-QSAR study of some novel 1,2,4-triazolo[4,3- a ]pyridine derivatives
    • DOI.
    • Liu, X. H.; Xu, X. Y.; Tan, C. X.; Weng, J. Q.; Chen, J. Synthesis, crystal structure, herbicidal activities and 3D-QSAR study of some novel 1,2,4-triazolo[4,3- a ]pyridine derivatives. Pest Manag. Sci. DOI: 10.1002/ps.3804.
    • Pest Manag. Sci.
    • Liu, X.H.1    Xu, X.Y.2    Tan, C.X.3    Weng, J.Q.4    Chen, J.5
  • 44
    • 84914172333 scopus 로고    scopus 로고
    • SYBYL 6.9, Tripos Associates, St. Louis, MO, USA.
    • SYBYL 6.9, Tripos Associates, St. Louis, MO, USA.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.