Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Gyula Mikite"'
Autor:
Gyula Mikite, István Ujváry
Publikováno v:
Organic Process Research & Development. 7:585-587
A practical synthesis of the tsetse fly attractant 3-n-propylphenol involves the Grignard reaction of 3-hydroxybenzaldehyde and ethylmagnesium bromide affording a benzylic alcohol-type phenol derivative that upon catalytic hydrogenation gives the tit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e50a682af711d8ba6e6397d5067fcaa
https://doi.org/10.1021/op0340309
https://doi.org/10.1021/op0340309
Autor:
A. Nagy, Laszlo Levai, Daniel Bozsing, Peter Toempe, Benko Pal, G. Lax, Eva Furdyga, Gyula Mikite
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7bc0ec795220a1b448de6e3440e6f6c
https://doi.org/10.1002/chin.199223179
https://doi.org/10.1002/chin.199223179
Publikováno v:
Pesticide Science. 35:237-242
A new series of compounds with high contra-selective activity against benomyl-resistant fungal strains was found among ring-substituted N-phenyl-anilines. Hydrophobic substitution in one of the benzene rings, together with the secondary amine charact
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68af73560af3bde3e6e3c87ee485f55d
https://doi.org/10.1002/ps.2780350307
https://doi.org/10.1002/ps.2780350307
Publikováno v:
Pesticide Science. 14:513-520
The structure-antifungal activity correlations of 23 new nitroalcohol derivatives (1-substituted-2-nitropropane-1, 3-diols, their ethers and esters) were investigated using a generalised quantitative structure-activity relationships (QSAR) method, co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02020f1b6d6870ec0d294c2982189d3b
https://doi.org/10.1002/ps.2780140509
https://doi.org/10.1002/ps.2780140509
Publikováno v:
Pesticide Science. 13:557-562
Thirty-six new nitro-alcohol derivatives were synthesised. Tested in vitro against Helminthosporium sativum, the compounds had high antifungal activities; the EC50 values varied between 10−2 and 10−6 M, and for the majority of the compounds betwe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::78240c52f2b7d165bdd9d9873b129aef
https://doi.org/10.1002/ps.2780130515
https://doi.org/10.1002/ps.2780130515
Publikováno v:
Journal of Chromatography A. 355:211-220
Reversed-phase charge-transfer thin-layer chromatography has been applied to study the interaction of the fungicide 1-phenyl-2-nitro-3-acetoxyprop-1-ene with amino acids and glutathione. The fungicide interacts preferentially with thiol amino acids a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::30c2577affe1719ca53ad025607ff3f0
https://doi.org/10.1016/s0021-9673(01)97317-0
https://doi.org/10.1016/s0021-9673(01)97317-0
Publikováno v:
Journal of Inclusion Phenomena. 4:55-59
Cyclodextrin complexation decreases the apparent lipophilicity of hydrophobic guest molecules. A higher complex stability results in a larger decrease of lipophilicity as determined by reversed-phase thin-layer chromatography. The method was applied
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de6b46db1e4c4bdf9d739a374c6a3cf6
https://doi.org/10.1007/bf00662081
https://doi.org/10.1007/bf00662081
Kinetics of the reaction of the first metabolite of fenitropan with some low molecular weight thiols
Publikováno v:
Pesticide Science. 26:253-259
2-Nitro-I-phenylpropen-3-yl acetate (NPPA), the first metabolite of the fungicide fenitropan, reacted readily with glutathione in aqueous ethanol solutions at room temperature, producing at least two products. The first reaction step, which is believ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eb7d32e5459d75b3e02e31d867c7474d
https://doi.org/10.1002/ps.2780260305
https://doi.org/10.1002/ps.2780260305