Vyhledat publikace
Wiedermannová, I.; Slouka, J.
Oxo derivatives of quinoxaline V. Synthesis of some arylhydrazones of 2-oxo-6,7-dichloro-1,2-dihydro-quinoxaline-3-carbaldehyde
Acta Univ. Palacki. Olomouc. Fac. Rerum.Nat. Chemica 2002, 53.
Wiedermannová, I.; Žídková, L.; Slouka, J.
Oxo derivatives of quinoxaline VI: Synthesis of some arylhydrazines of 6,7-disubstituted-1,2-dihydro-quinoxaline-3-carbaldehyde
Acta Univ. Palacki. Olomouc. Fac. Rerum.Nat. Chemica 2002, 59.
Wiedermannová, I.; Slouka, J.; Lemr, K.
An anomalous course of the condensation of 1,5-diaryl-3-formazyl glyoxylic acids with o-phenylenediamine. A simple synthesis of some benzimidazole-2-carboxamidarylhydrazones
Heterocyclic Commun 2002, 479.
Gucký, T.; Nálepa, K.; Wiedermannová, I.
Synthesis of the new serie of novel heterocyclic skeleton isoxazolo[4,5-e] 1,2,4-triazines and new serie of the pyrazolo[4,3-e]1,2,4-triazines
Heterocyclic Commun 2002, 613.
Bílek, P.; Slouka, J.
Synthesis of some symmetrically substituted compounds derived from 1,3-bis(6-azauracil-1-yl)benzene and 1,3,5-tris(6-azauracil-1-yl)benzene [1]
J. Heterocyclic Chem 2002, 357.
Stýskala, J.; Lyčka, A.; Slouka, J.
Synthesis of some [1,2,4]triazino[5,6-b]quinoline derivatives [1]
J. Heterocyclic Chem 2002, 1309.
Cankař, P.; Wiedermannová, I.; Slouka, J.
Heterocyclic amines I: The cycloaddition reaction of malonodinitrileand some of its derivatives with hydrazine and their use for thepreparation of 3,5-diamino-4-arylazopyrazoles derived fromsulfonamides.““
Acta Univ. Palacki. Olomuc., Fac.Rerum. Nat., Chemica““ 2002, 7-15.
Bílek, P.; Slouka, J.
Cyclocondensation reactions of heterocyclic carbonyl compounds VII. Synthesis of some substituted benzo-[1,2,4]triazino[2,3-a]benzimidazoles
Heterocyclic Commun 2002, 123.
Zedníková, G.; Nálepa, K.; Gucký, T.
Synthesis of some new 3,5,7-trisubstituted pyrazolo[4,3-e]1,2,4-triazines.
Heterocycl.Communn. 2001, 4 , 349.
Nálepa, K.; Gucký, T.
Synthesis of some new pyrazolo[4,3-e]1,2,4-triazines.
Acta Univ.Palacki.OlomoucFac.Rer.Nat.Chemica 2001, 49.