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Volumn 58, Issue 5, 2010, Pages 2685-2689

Design, synthesis, and herbicidal activities of novel 2-cyanoacrylates containing isoxazole moieties

Author keywords

Cyanoacrylates; Herbicidal activity; Isoxazole; PSII electron transfer inhibitor

Indexed keywords

CYANOACRYLATE DERIVATIVE; HERBICIDE;

EID: 77949366852     PISSN: 00218561     EISSN: 15205118     Source Type: Journal    
DOI: 10.1021/jf902541w     Document Type: Article
Times cited : (58)

References (18)
  • 1
    • 10244278389 scopus 로고
    • Cyanoacrylate inhibitors of photosynthetic electron transport. Structural requirements for inhibitor potency and herbicidal activity
    • Baker, D. R, Fenyes, J. G, Steffens, J. J, Eds, Maple Press: New York
    • Huppatz, J. L.; McFadden, H. G.; Huber, M.-L.; McCaffery, L. F. Cyanoacrylate inhibitors of photosynthetic electron transport. Structural requirements for inhibitor potency and herbicidal activity. In Synthesis and Chemistry of Agrochemicals III; Baker, D. R., Fenyes, J. G., Steffens, J. J., Eds.; Maple Press: New York, 1992; pp 186-199.
    • (1992) Synthesis and Chemistry of Agrochemicals III , pp. 186-199
    • Huppatz, J.L.1    McFadden, H.G.2    Huber, M.-L.3    McCaffery, L.F.4
  • 2
    • 0042061123 scopus 로고    scopus 로고
    • Synthesis and herbicidal activity of 2-cyano-3-substitutedpyridinemethylaminoacrylates
    • Wang, Q. M.; Sun, H. K.; Cao, H. Y.; Cheng, M. R.; Huang, R. Q. Synthesis and herbicidal activity of 2-cyano-3-substitutedpyridinemethylaminoacrylates. J. Agric. Food Chem. 2003, 51, 5030-5035.
    • (2003) J. Agric. Food Chem , vol.51 , pp. 5030-5035
    • Wang, Q.M.1    Sun, H.K.2    Cao, H.Y.3    Cheng, M.R.4    Huang, R.Q.5
  • 3
    • 15944403576 scopus 로고    scopus 로고
    • Synthesis and herbicidal activity of 2-cyano-3-(2-fluoro-5-pyridyl)- methylaminoacrylates
    • Liu, Y. X.; Zhao, Q. Q.; Wang, Q. M.; Li, H.; Huang, R. Q.; Li, Y. H. Synthesis and herbicidal activity of 2-cyano-3-(2-fluoro-5-pyridyl)- methylaminoacrylates. J. Fluorine Chem. 2005, 126, 345-348.
    • (2005) J. Fluorine Chem , vol.126 , pp. 345-348
    • Liu, Y.X.1    Zhao, Q.Q.2    Wang, Q.M.3    Li, H.4    Huang, R.Q.5    Li, Y.H.6
  • 4
    • 1842587831 scopus 로고    scopus 로고
    • Synthesis and herbicidal activity of 2-cyano-3-(2-chlorothiazol-5-yl)methyl-aminoacrylates
    • Wang, Q. M.; Li, H.; Cao, H. Y.; Li, Y. H.; Huang, R. Q. Synthesis and herbicidal activity of 2-cyano-3-(2-chlorothiazol-5-yl)methyl-aminoacrylates. J. Agric. Food Chem. 2004, 52, 1918-1922.
    • (2004) J. Agric. Food Chem , vol.52 , pp. 1918-1922
    • Wang, Q.M.1    Li, H.2    Cao, H.Y.3    Li, Y.H.4    Huang, R.Q.5
  • 5
    • 34247621194 scopus 로고    scopus 로고
    • Synthesis, crystal structure, and biological activities of 2-cyanoacrylates containing furan or tetrahydrofuran moieties
    • Liu, Y. X; Cai, B. L.; Li, Y. H.; Song, H. B.; Huang, R. Q.; Wang, Q. M. Synthesis, crystal structure, and biological activities of 2-cyanoacrylates containing furan or tetrahydrofuran moieties. J. Agric. Food Chem. 2007, 55, 3011-3017.
    • (2007) J. Agric. Food Chem , vol.55 , pp. 3011-3017
    • Liu, Y.X.1    Cai, B.L.2    Li, Y.H.3    Song, H.B.4    Huang, R.Q.5    Wang, Q.M.6
  • 7
    • 34748899444 scopus 로고    scopus 로고
    • Binding model and 3D-QSAR of 3-(2-chloropyrid-5-ylmethylamino)-2-cyanoacrylates as PSII electron transport inhibitor
    • Han, X. F.; Liu, Y. X.; Liu, Y.; Lai, L. H.; Huang, R. Q.; Wang, Q. M. Binding model and 3D-QSAR of 3-(2-chloropyrid-5-ylmethylamino)-2-cyanoacrylates as PSII electron transport inhibitor. Chin. J. Chem. 2007, 25, 1135-1138.
    • (2007) Chin. J. Chem , vol.25 , pp. 1135-1138
    • Han, X.F.1    Liu, Y.X.2    Liu, Y.3    Lai, L.H.4    Huang, R.Q.5    Wang, Q.M.6
  • 8
    • 64549147543 scopus 로고    scopus 로고
    • Design, synthesis, and biological activities of novel 2-cyanoacrylates containing oxazole, oxadiazole, or quinoline moieties
    • Zhao, Q. Q.; Liu, S. H.; Li, Y. H.; Wang, Q. M. Design, synthesis, and biological activities of novel 2-cyanoacrylates containing oxazole, oxadiazole, or quinoline moieties. J. Agric. Food Chem. 2009, 57, 2849-2855.
    • (2009) J. Agric. Food Chem , vol.57 , pp. 2849-2855
    • Zhao, Q.Q.1    Liu, S.H.2    Li, Y.H.3    Wang, Q.M.4
  • 9
    • 26444547640 scopus 로고    scopus 로고
    • Synthesis and bioactivity of fluorine compounds containing isoxazolylamino and phosphonate groups
    • Song, B. A.; Yang, S.; Hong, Y. P.; Zhang, G. P.; Jin, L. H.; Hu, D. Y. Synthesis and bioactivity of fluorine compounds containing isoxazolylamino and phosphonate groups. J. Fluorine Chem. 2005, 126, 1419-1424.
    • (2005) J. Fluorine Chem , vol.126 , pp. 1419-1424
    • Song, B.A.1    Yang, S.2    Hong, Y.P.3    Zhang, G.P.4    Jin, L.H.5    Hu, D.Y.6
  • 10
    • 27844538344 scopus 로고    scopus 로고
    • Furans, thiophenes and related heterocycles in drug discovery
    • Sperry, J.; Wright, D. Furans, thiophenes and related heterocycles in drug discovery. Curr. Opin. Drug Discov. Dev. 2005, 8, 723-740.
    • (2005) Curr. Opin. Drug Discov. Dev , vol.8 , pp. 723-740
    • Sperry, J.1    Wright, D.2
  • 11
    • 38949101931 scopus 로고    scopus 로고
    • Studies of nitrile oxide cycloadditions, and the phenolic oxidative coupling of vanillin aldoxime by Geobacillus sp. DDS012 from Italian rye grass silage
    • Kelly, D. R.; Baker, S. C.; King, D. S.; de Silva, D. S.; Lord, G.; Taylor, J. P. Studies of nitrile oxide cycloadditions, and the phenolic oxidative coupling of vanillin aldoxime by Geobacillus sp. DDS012 from Italian rye grass silage. Org. Biomol. Chem. 2008, 6 (4), 787-796.
    • (2008) Org. Biomol. Chem , vol.6 , Issue.4 , pp. 787-796
    • Kelly, D.R.1    Baker, S.C.2    King, D.S.3    de Silva, D.S.4    Lord, G.5    Taylor, J.P.6
  • 13
    • 1542427731 scopus 로고    scopus 로고
    • Synthesis of dithiaand tetrathiacyclophanes incorporating isoxazole units
    • Hatta, T.; Kawano, M.; Maeda, H.; Tsuge, O. Synthesis of dithiaand tetrathiacyclophanes incorporating isoxazole units. J. Heterocycl. Chem. 1997, 34 (2), 579-583.
    • (1997) J. Heterocycl. Chem , vol.34 , Issue.2 , pp. 579-583
    • Hatta, T.1    Kawano, M.2    Maeda, H.3    Tsuge, O.4
  • 14
    • 0008917420 scopus 로고
    • Conversion of 2-isoxazolines to isoxazoles
    • Bianchi, G.; Grünanger, P. Conversion of 2-isoxazolines to isoxazoles. Tetrahedron 1965, 21, 817-822.
    • (1965) Tetrahedron , vol.21 , pp. 817-822
    • Bianchi, G.1    Grünanger, P.2
  • 15
    • 0013906073 scopus 로고
    • 3-Aryl-5- halomethylisoxazoles. A new class of anthelmintics
    • Sen, H. G.; Seth, D.; Joshi, U. N.; Rajagopalan, P. 3-Aryl-5- halomethylisoxazoles. A new class of anthelmintics. J. Med. Chem. 1966, 9 (3), 431-433.
    • (1966) J. Med. Chem , vol.9 , Issue.3 , pp. 431-433
    • Sen, H.G.1    Seth, D.2    Joshi, U.N.3    Rajagopalan, P.4
  • 16
    • 0007170782 scopus 로고
    • One pot synthesis of 3-chloro-5-substituted isoxazoles by 1,3-dipolar cycloaddition
    • Chiarino, D.; Napoletano, M.; Sala, A. One pot synthesis of 3-chloro-5-substituted isoxazoles by 1,3-dipolar cycloaddition. Synth. Commun. 1988, 18 (10), 1171-1176.
    • (1988) Synth. Commun , vol.18 , Issue.10 , pp. 1171-1176
    • Chiarino, D.1    Napoletano, M.2    Sala, A.3
  • 17
    • 0027363856 scopus 로고
    • Regioselective syntheses of 3-aminomethyl-5-substituted isoxazoles: A facile and chemoselective reduction of azide to amine by sodium borohydride using 1,3-propanedithiol as a catalyst
    • Pei, Y.; Wickham, B. O. S. Regioselective syntheses of 3-aminomethyl-5-substituted isoxazoles: A facile and chemoselective reduction of azide to amine by sodium borohydride using 1,3-propanedithiol as a catalyst. Tetrahedron Lett. 1993, 34 (47), 7509-7512.
    • (1993) Tetrahedron Lett , vol.34 , Issue.47 , pp. 7509-7512
    • Pei, Y.1    Wickham, B.O.S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.