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Autor:
L. Kaczmarek, P. Nantka‐Namirski
Publikováno v:
ChemInform. 22
Publikováno v:
ChemInform. 23
Selective, mild and safe N-oxidation of N-heteroaromatic compounds and tertiary amines affording high product yields was achieved by using the H2O2-urea/phthalic anhydride system.
Publikováno v:
ChemInform. 23
The use of the system hydrogen peroxide-urea/phthalic anhydride in the safe oxidation of dialkyl, diaryl and alkyl aryl sulfides under mild conditions is reported. The corresponding sulfoxides are formed in excellent yields.
Publikováno v:
ChemInform. 25
Publikováno v:
Polish journal of pharmacology and pharmacy. 43(5)
The synthesis of two isomeric dipyrido[1,3]diazepinones (3a,4) and N-monosubstituted derivatives of 3a by cyclocondensation of corresponding bipyridinediamines (1, 2) with urea was described. The alkylation of 3a and 4 with alkyl halides 6 in K2CO3/D
Publikováno v:
Polish journal of pharmacology and pharmacy. 42(2)
The synthesis and properties of 13H-naphtho[1',2':7,6] [1,4] diazepino[2,3-b] pyridines (7a--g) were described. New compounds were studied in rats and in mice in the tests used for preclinical assessment of antidepressant or anxiolytic activity. Comp
Publikováno v:
Polish journal of pharmacology and pharmacy. 42(1)
The one-pot synthesis and properties of some derivatives of 3-phenylimidazo [4,5-b]pyridine (4a-g) were described. The central action of compounds 4a, 4f and 4g has been investigated using behavioral tests in mice and rats. The tested compounds showe
Publikováno v:
Liebigs Annalen der Chemie. 1992:883-884
The use of the system hydrogen peroxide-urea/phthalic anhydride in the safe oxidation of dialkyl, diaryl and alkyl aryl sulfides under mild conditions is reported. The corresponding sulfoxides are formed in excellent yields.
Autor:
Graham A. Webb, L. Kaczmarek, J. J. Basselier, Lech Stefaniak, P. Nantka-Namirski, D. Davoust
Publikováno v:
Magnetic Resonance in Chemistry. 23:853-855
15N NMR spectroscopy was used to distinguish between isomers and to characterize some series of novel fused polyaza heterocyclic ring systems. Support for the assignments was provided by means of some INDO/S-SOS shielding calculations. Previously obs