Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Garavaglia, Carlo"'
Publikováno v:
ChemInform. 23
Pure stereoisomers of two new triazole and morpholine fungicides were prepared starting from enzymatically synthesized chiral alcohols intermediates. Two resolution strategies were compared: lipase-catalyzed hydrolysis of corresponding acetates in wa
Autor:
Luigi Mirenna, Garavaglia Carlo, Sandro Spezia, Paolo Golini, Pietro Cesti, Lucio Filippini, Daniele Bianchi
Publikováno v:
Journal of Agricultural and Food Chemistry. 40:1989-1992
Four optically pure stereoisomers of 2,6-dimethyl-4-[2-methyl-3-[3-(cyclopropylmethoxy)phenyl]propyl]-morpholine (1), a new broad-spectrum morpholine fungicide, were prepared starting from the chiral precursor 2-methyl-3-[3-(benzyloxy)phenyl]-1-propa
Publikováno v:
Pure and Applied Chemistry. 64:1073-1078
Pure stereoisomers of two new triazole and morpholine fungicides were prepared starting from enzymatically synthesized chiral alcohols intermediates. Two resolution strategies were compared: lipase-catalyzed hydrolysis of corresponding acetates in wa
Publikováno v:
Pesticide Biochemistry and Physiology. 40:68-79
Quantitative structure-activity relationships have been performed by applying the Hansch approach to a series of known and new antifungal azoles, mainly 1,2,4-triazole derivatives, in their control of two diseases, caused by Erysiphe graminis and Puc
Publikováno v:
Journal of Agricultural and Food Chemistry. 39:197-201
Both enantiomers of (R,S)-2-(2,4-dichlorophenyl)-3-(1H-1,2,4-triazol-1-yl)propyl 1,1,2,2-tetrafluoroethyl ether (tetraconazole), a new, broad spectrum, triazole fungicide, were prepared by stereoselective lipase-catalyzed hydrolysis of the racemic pr
Publikováno v:
Pure & Applied Chemistry; January 1992, Vol. 64 Issue: 8 p1073-1078, 6p
Publikováno v:
In Pesticide Biochemistry and Physiology 1991 40(1):68-79