Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Lubomír Zalibera"'
Autor:
V. Kratky, Magdaléna Štolcová, Milan Hronec, Milan Králik, Miroslava Mecárová, Lubomír Zalibera, Alexander Kaszonyi
Publikováno v:
Collection of Czechoslovak Chemical Communications. 68:1819-1832
Liquid phase hydrogenation of chloronitrobenzenes to corresponding chloroanilines over Pd on carbon (Pd/C) under mild reaction conditions was studied. On the basis of 1H, 13C NMR, GC-MS and HPLC analyses of reaction mixtures, the reaction pathways we
Publikováno v:
Applied Catalysis A: General. 235:225-231
The liquid phase hydrogenation of chloronitrobenzene isomers ( x -CNB, x =2, 3, 4) to corresponding chloroanilines ( x -CAN) at 0.5 MPa and 25 °C was studied. Palladium catalysts containing 1 wt.% of Pd on charcoal and sulphonated poly(styrene- co -
Publikováno v:
Collection of Czechoslovak Chemical Communications. 60:605-611
Condensation reactions of 1,2,3,4-tetrahydro-6-methyl-2,4-dioxo-5-pyrimidinecarbaldehyde with nine acid derivatives containing an active methylene group are described. The obtained products were characterized by their IR, UV, 1H NMR, 13C NMR and mass
Publikováno v:
Collection of Czechoslovak Chemical Communications. 60:583-593
The Gould-Jacobs reaction of all position isomeric 2-aminonitrobenzothiazoles II with diethyl ethoxy- methylenemalonate has been studied. The structure of substitution (IV) and cyclization (VI) products and of the corresponding acids (VIII) was confi
Publikováno v:
Collection of Czechoslovak Chemical Communications. 59:1145-1152
Thermal cyclocondensation of starting ethyl (1-methyl-5- and 6-benzimidazolyl/benzotriazolyl)aminomethylenepropanedioates (Ia - Ie) in aprotic medium gives angularly condensed ethyl azolo[4,5-f]quinolonecarboxylates IIa, IIc, IIe and azolo[5,4-f]quin
Publikováno v:
Collection of Czechoslovak Chemical Communications. 59:1458-1462
Substituted 2-amino-3-cyano-4H-pyrans represent important precursors in syntheses of condensed heterocycles containing a 4H-pyran nucleus. In the context of studies of reactivity of 2-amino-5-acetyl-4-(5-X-2-furyl)-3-cyano-6-methyl-4H-pyrans we were
Publikováno v:
Collection of Czechoslovak Chemical Communications. 59:444-452
The reaction of 5-X-2-furaldehydes (X = C6H5, COOCH3, COOC2H5, C6H5O, C6H5S, CH3S, 4-Cl-C6H4S, CH3SO2, C6H5SO2, 4-Cl-C6H4SO2) with ethyl cyanoacetate in dry ethanol catalyzed by sodium ethoxide yielded the corresponding ethyl 2-cyano-3-(5-X-2-furyl)a
Publikováno v:
Collection of Czechoslovak Chemical Communications. 58:555-564
(E-2-Formyl-3-(2-furyl)propenenitrile (I) reacts with primary aromatic amines under formation of 3-(arylamino)-2-[5-(arylamino)-2-oxo-3-cyclopenten-1-yl]propenenitriles (IVa-IVi). Condensation of I with salts of nitrogen bases in pyridine affords 2-(
Publikováno v:
ChemInform. 25
Publikováno v:
ChemInform. 25