Ebert, E.; Eckhardt, W.; Jaekel, K.; Moser, P.; Sozzi, D.; Vogel, C. published the artcile< Quantitative structure activity relationships of fungicidally active triazoles: analogs and stereoisomers of propiconazole and etaconazole>, Electric Literature of 112-63-0, the main research area is fungicide triazole derivative structure ergosterol; propiconazole stereoisomer fungicide sterol metabolism; ectaconazole stereoisomer fungicide sterol metabolism; QSAR triazole fungicide.
The preparation of the 4 stereoisomers of propiconazole (TILT) is described. Their inhibition of the 14α-C-demethylation of the sterol nucleus is examined and compared with the inhibition by the four stereoisomers of etaconazole (SONAX). The quant. structure-activity relationships (QSAR) of substituted 1,3-dioxolane-2-yl-methyltriazoles and 1,3-dioxane-2-yl-methyltriazoles on in vivo fungicidal activity are investigated.
Zeitschrift fuer Naturforschung, C: Journal of Biosciences published new progress about Agrochemical fungicides. 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, Electric Literature of 112-63-0.
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Ester – Wikipedia,
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