76714-84-6Relevant articles and documents
Synthesis and fungicidal activity of (1Z, 3Z)-4,4-dimethyl-1- substitutedphenyl-2-(1H-1,2,4-triazol-1-yl)-pent-1-en-3-one O-[2,4- dimethylthiazole(or 4-methyl-1,2,3-thiadiazole)]-5-carbonyl oximes
Mao, Hui-Yu,Song, Hong,Shi, De-Qing
scheme or table, p. 511 - 515 (2012/09/08)
A series of novel (Z)-1-tert-butyl (or phenyl)-2-(1H-1,2,4-triazol-1-yl)- ethanone O-[2,4-dimethylthiazole (or 4-methyl-1,2,3-thiadiazole) -5-carbonyl] oximes 5a-5c and (1Z, 3Z)-4,4-dimethyl-1-substitutedphenyl-2-(1H-1,2,4-triazol- 1-yl)-pent-1-en-3-one O-[2,4-dimethylthiazole (or 4-methyl-1,2,3-thiadiazole)-5- carbonyl] oximes 6a-6e were synthesized by the condensations of (Z)-1-tert-butyl (or phenyl)-2-(1H-1,2,4-triazol-1-yl)-ethanone oximes 3 or (1Z, 3Z)-4,4-dimethyl-1-substitutedphenyl-2-(1H-1,2,4-triazol-1-yl)-pent-1-en-3-one oximes 4 with 2,4-dimethylthiazole-5-carbonyl chloride or 4-methyl-1,2,3- thiadiazole-5-carbonyl chloride in the basic condition. Their structures were confirmed by IR, 1H NMR, mass spectroscopy, and elemental analyses. The results of preliminary bioassays showed the title compounds 5 and 6 exhibited moderate to good fungicidal activities. For example, compound 6c possessed 86.4% inhibition against Fusarium oxysporum, and compound 6b exhibited 86.4 and 100% inhibition against Fusarium oxysporum and Cercospora arachidicola Hori at the concentration of 50 mg/L, respectively.
Geometrical isomer of 1-substituted-1-triazolylstyrenes, and their production and use as fungicide, herbicide and/or plant growth regulant
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, (2008/06/13)
The present invention relates to one of the two geometrical isomers (a compound defined as I-A isomer in the description below) of a triazole compound represented by the formula (I) or (II), STR1 wherein R1 is a hydrogen atom, a C1 -