Synthesis and herbicidal activity of novel heterocyclic protoporphyrinogen oxidase inhibitors
Meazza G., Bettarini F., La Porta P., Piccardi P., Signorini E., Portoso D., Fornara L. (2004) Synthesis and herbicidal activity of novel heterocyclic protoporphyrinogen oxidase inhibitors. Pest Manag Sci 60 : 1178 1188.
Crystal structure of protoporphyrinogen IX oxidase: A key enzyme in haem and chlorophyll biosynthesis
Koch M., Breithaupt C., Kiefersauer R., Freigang J., Huber R., Messerschmidt A. (2004) Crystal structure of protoporphyrinogen IX oxidase: a key enzyme in haem and chlorophyll biosynthesis. EMBO J 23 : 1720 1728.
Protoporphyrinogen IX-oxidizing activities involved in the mode of action of a new compound N-[4-chloro-2-fluoro-5-{3-(2-fluorophenyl)-5-methyl-4,5- ihydroisoxazol-5-yl-methoxy}-phenyl]-3,4,5,6-tetrahydrophthalimide
Hwang I.T., Hong K.S., Choi J.S., Kim H.R., Joen D.J., Cho K.Y. (2004) Protoporphyrinogen IX-oxidizing activities involved in the mode of action of a new compound N-[4-chloro-2-fluoro-5-{3-(2-fluorophenyl)-5-methyl-4,5- ihydroisoxazol-5-yl-methoxy}-phenyl]-3,4,5,6-tetrahydrophthalimide. Pestic Biochem Physiol 80 : 123 130.
Discovery and development of a commercial synthesis of azafenidin
Shapiro R., DiCosimo R., Hennessey S.M., Stieglitz B., Campopiano O., Chiang G.C. (2001) Discovery and development of a commercial synthesis of azafenidin. Org Process Res Dev 5 : 593 598.
Preparation of 1-carbamoyl-3-(cyclo)alkyl-4-amino-1,2,4-triazolin-5-ones as herbicides
DE 3 839 206.
Muller K.H., Lindig M., Findeisen K., Konig K., Lurssen K., Santel H.J., Schmidt R.R., Strang H. (1990) Preparation of 1-carbamoyl-3-(cyclo)alkyl-4- amino-1,2,4-triazolin-5-ones as herbicides. DE 3 839 206. Chem Abstr 113 : 172023.
Synthesis bioactivity theoretical and molecular docking study of 1-cyano-N-substituted-cyclopropanecarboxamide as ketol-acid reductoisomerase inhibitor
Liu X.H., Chen P.Q., Wang B.L., Li Y.H., Wang S.H., Li Z.M. (2007) Synthesis bioactivity theoretical and molecular docking study of 1-cyano-N-substituted-cyclopropanecarboxamide as ketol-acid reductoisomerase inhibitor. Bioorg Med Chem Lett 17 : 3784 3788.
Structure bioactivity and theoretical study of 1-cyano-N-p-tolylcyclo- propanecarboxamide
Liu X.H., Chen P.Q., He F.Q., Li Y.H., Wang S.H., Li Z.M. (2007) Structure bioactivity and theoretical study of 1-cyano-N-p-tolylcyclo- propanecarboxamide. Struct Chem 5 : 563 568.
Synthesis bioactivity and SAR study of N′-(5-substituted-1,3,4- thiadiazol-2-yl)-N-cyclopropyformyl-thiourea as ketol-acid reductoisomerase inhibitor
Liu X.H., Zhang C.Y., Guo W.C., Li Y.H., Chen P.Q., Wang T., Dong W.L., Sun H.W., Li Z.M. (2009) Synthesis bioactivity and SAR study of N′-(5-substituted-1,3,4-thiadiazol-2-yl)-N-cyclopropyformyl-thiourea as ketol-acid reductoisomerase inhibitor. J Enzym Inhib Med Chem 24 : 545 552.
Synthesis of some N,N′-diacylhydrazine derivatives with radical scavenging and antifungal activity
Liu X.H., Shi Y.X., Ma Y., He G.R., Dong W.L., Zhang C.Y., Wang B.L., Wang S.H., Li B.J., Li Z.M. (2009) Synthesis of some N,N′-diacylhydrazine derivatives with radical scavenging and antifungal activity. Chem Biol Drug Des 73 : 320 327.
Synthesis, antifungal activities and 3D-QSAR study of N-(5-substituted-1,3,4-thiadiazol-2-yl)cyclopropanecarboxamides
DOI:.
Liu X.H., Shi Y.X., Ma Y., Zhang C.Y., Dong W.L., Li P., Wang B.L., Li B.J., Li Z.M. (2009) Synthesis, antifungal activities and 3D-QSAR study of N-(5-substituted-1,3,4-thiadiazol-2-yl)cyclopropanecarboxamides. Eur J Med Chem DOI :.
Wang L., Wang B.L., Li Z.M., Song H.B. (2006) 2-(2,4-Dichlorophenyl)-5- methyl-4-(2-nitrophenylsulfonyl)-2H-1,2,4-triazol-3(4H)-one. Acta Crystallogr E 62 : O935.