• Title/Summary/Keyword: N-phenyl-3,4,5,6-tetrahydrophthalimides

Search Result 3, Processing Time 0.017 seconds

Comparative molecular field analyses(CoMFA) on the growth inhibition activity of N-phenyl-3,4,5,6-tetrahydrophthalimide and N-phenyl-3,4-dimethylmaleimide Derivatives (N-치환 phenyl-3,4,5,6-tetrahydrophthalimide와 N-치환 phenyl-3,4-dimethylmaleimide 유도체의 생장 저해활성에 관한 l 분자장 분석 (CoMFA))

  • Sung, Nack-Do;Ock, Hwan-Suk;Song, Jong-Hwan;Lee, Yong-Gu
    • The Korean Journal of Pesticide Science
    • /
    • v.7 no.2
    • /
    • pp.75-82
    • /
    • 2003
  • We discuss that the growth inhibition activities against root and shoot of rice plant (Oryza sativa L.) and barnyard grass (Echinochloa crus-galli) by N-phenyl-3,4,5,6-tetrahydrophthalimide (A) and N-phenyl-3,4-dimethylmaleimide (B) derivatives with changing substituents can be explained and predicted using comparative molecular field analyses (CoMPA) method. And the results show that the cross-validation value, $q^2$ at three components and Pearson correlation coefficient, $r^2$ were rice plant: shoot; $r^2=0.987$, $q^2=0.387$ & root; $r^2=0.923$, $q^2=0.307$ and barnyard grass: shoot; $r^2=0.902$, $q^2=0.535$ & root; $r^2=0.900$, $q^2=0.450$, respectively. In addition, The activities of unknown compounds were predicted by CoMFA method. From the contour map of (A) derivatives, the selective factors to remove barnyard grass takes positive charge on the benzylic carbon atom (C27), negative charged carbon atom (C29) of meta position and steric bulky groups on the cyclic imino ring (C7-C8).

Synthesis and herbicidal activities of 3,4,5,6-tetrahydrophthalimides substituted with pyrimidines (피리미딘이 치환된 3,4,5,6-tetrahydrophthalimide 유도체의 합성과 제초활성)

  • Ryu, Jae-Wook;Lee, Min-Ju;Chung, Kun-Hoe;Ko, Young-Kwan;Woo, Jae-Chun;Koo, Dong-Wan;Kim, Tae-Joon;Cho, Jung-Sub;Kim, Dae-Whang
    • The Korean Journal of Pesticide Science
    • /
    • v.10 no.4
    • /
    • pp.262-265
    • /
    • 2006
  • A series of N-[4-chloro-2-fluoro-5-(2-(substituted)pyrimidinyloxy)phenyl]-3,4,5,6-tetrahydrophthalimides was synthesized, and the herbicidal activities of those derivatives were evaluated through pre- and post-emergence application under upland conditions in a greenhouse. The results showed that most compounds resulted in stronger herbicidal activities on broadleaf weeds than on grass weeds. The N-[4-chloro-2-fluoro-5-(2-pyrimidinyloxy)phenyl]-3,4,5,6-tetrahydrophthalimide showed the best weed control efficacy and marginal corn safety at a rate of 60 g/ha through pre-emergence application.

Synthesis and herbicidal activities of N-[4-Cyano-2-fluoro-5-(substituted)phenyl]-3,4,5,6-tetrahydrophthalimide (N-[4-Cyano-2-fluoro-5-(substituted)phenyl]-3,4,5,6-tetrahydrophthalimide 유도체의 합성과 제초활성)

  • Ryu, Jae-Wook;Chung, Kun-Hoe;Ko, Young-Kwan;Woo, Jae-Chun;Koo, Dong-Wan;Kim, Tae-Joon;Choi, Jung-Sub;Park, Chae-Hyun;Kim, Dae-Whang
    • The Korean Journal of Pesticide Science
    • /
    • v.9 no.1
    • /
    • pp.108-111
    • /
    • 2005
  • A series of N-[4-cyano-2-fluoro-5-(2-pyrimidinyloxy, 2-benzyloxy or 2-pyridinyloxy)phenyl]-3,4,5,6-tetrahydrophthalimides was synthesized, and the herbicidal activities of those deivatives were evaluated through pre- and post-emergence application under upland conditions in a greenhouse. The results showed that most compounds resulted in stronger herbicidal activity on broadleaf weeds than on grass weeds and higher through post-emergence than pre-emergence application. The N-[(4-cyano-2-fluoro-5-(2-pyrimidinyloxy) phenyl]-3,4,5,6-tetrahydrophthalimide showed the best weed control efficacy and marginal corn safety at a rate of 60 g/ha through pre-emergence application.