Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Luigi Mirenna"'
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f970398da5014f7fed5c3fa2a58e768f
https://doi.org/10.1002/chin.199242267
https://doi.org/10.1002/chin.199242267
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bfbc6eda041d4a58995c819166bf3fe6
https://doi.org/10.1021/jf00022a051
https://doi.org/10.1021/jf00022a051
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::39d3b6e25bc044b68ffe697be8ae8532
https://doi.org/10.1351/pac199264081073
https://doi.org/10.1351/pac199264081073
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b4d0cb52b9e45308a2d45b35ee767251
https://doi.org/10.1016/0048-3575(91)90049-r
https://doi.org/10.1016/0048-3575(91)90049-r
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b37f8484f81460632c0d0cec8abbc8f5
https://doi.org/10.1021/jf00001a040
https://doi.org/10.1021/jf00001a040