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Pischel, Helmut, Holý, Antonín, Veselý, Jiří, Wagner, Günther, Cech, Dieter (1982) Synthesis and biological activity of N-substituted 5-fluorouracil-1-acetamides. Collection of Czechoslovak Chemical Communications, 47. 2806-2813 doi:10.1135/cccc19822806

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Reference TypeJournal (article/letter/editorial)
TitleSynthesis and biological activity of N-substituted 5-fluorouracil-1-acetamides
JournalCollection of Czechoslovak Chemical Communications
AuthorsPischel, HelmutAuthor
Holý, AntonínAuthor
Veselý, JiříAuthor
Wagner, GüntherAuthor
Cech, DieterAuthor
Year1982Volume47
PublisherInstitute of Organic Chemistry & Biochemistry
DOIdoi:10.1135/cccc19822806Search in ResearchGate
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Mindat Ref. ID4385897Long-form Identifiermindat:1:5:4385897:6
GUID0
Full ReferencePischel, Helmut, Holý, Antonín, Veselý, Jiří, Wagner, Günther, Cech, Dieter (1982) Synthesis and biological activity of N-substituted 5-fluorouracil-1-acetamides. Collection of Czechoslovak Chemical Communications, 47. 2806-2813 doi:10.1135/cccc19822806
Plain TextPischel, Helmut, Holý, Antonín, Veselý, Jiří, Wagner, Günther, Cech, Dieter (1982) Synthesis and biological activity of N-substituted 5-fluorouracil-1-acetamides. Collection of Czechoslovak Chemical Communications, 47. 2806-2813 doi:10.1135/cccc19822806
In(1982) Collection of Czechoslovak Chemical Communications Vol. 47. Institute of Organic Chemistry & Biochemistry

See Also

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Pischel, Helmut, Holý, Antonín, Veselý, Jiří, Wagner, Günther, Cech, Dieter (1987) Hydrophilic 1-(carboxymethyl)-5-fluorouracil amides: Preparation and cytostatic activity. Collection of Czechoslovak Chemical Communications, 52. 2061-2069 doi:10.1135/cccc19872061
Pischel, Helmut, Holý, Antonín, Veselý, Jiří, Wagner, Günther (1984) Preparation and biological effects of N-tris(hydroxymethyl)methylaminocarbonylmethyl derivatives of heterocyclic bases. Collection of Czechoslovak Chemical Communications, 49. 2541-2550 doi:10.1135/cccc19842541
Holý, Antonín, König, Joachim, Veselý, Jiří, Cech, Dieter, Votruba, Ivan, De Clercq, Erik (1987) 5'-O-Alkyl-5-fluorouridines: Synthesis and biological activity. Collection of Czechoslovak Chemical Communications, 52. 1589-1608 doi:10.1135/cccc19871589
Pischel, Helmut, Holý, Antonín, Wagner, Günther (1979) Synthesis of conjugates of 5-halouracils with proteins using activated esters. Collection of Czechoslovak Chemical Communications, 44. 1634-1641 doi:10.1135/cccc19791634
Pischel, Helmut, Holý, Antonín, Wagner, Günther (1979) Synthesis of conjugates of 1-(carboxymethyl)cytosine and 1-(5-O-carboxymethyl-β-D-arabinofuranosyl)cytosine with proteins. Collection of Czechoslovak Chemical Communications, 44. 3023-3032 doi:10.1135/cccc19793023
Pischel, Helmut, Holý, Antonín, Wagner, Günther (1980) Synthesis of conjugates of 5'-O-carboxymethyl-5-halogeno-2'-deoxyuridines and 5'-O-carboxymethyl-5-halogenouridines with proteins. Collection of Czechoslovak Chemical Communications, 45. 606-610 doi:10.1135/cccc19800606
Pischel, Helmut, Holý, Antonín, Wagner, Günther (1981) Preparation of conjugates of uridine with proteins by the imido ester condensation method. Collection of Czechoslovak Chemical Communications, 46. 933-940 doi:10.1135/cccc19810933
Schwarz, Beatrice, Cech, Dieter, Holý, Antonín, Škoda, Jan (1980) Preparation, antibacterial effects and enzymatic degradation of 5-fluorouracil nucleosides. Collection of Czechoslovak Chemical Communications, 45. 3217-3230 doi:10.1135/cccc19803217
PISCHEL, H., HOLY, A., VESELY, J., WAGNER, G., CECH, D. (1983) ChemInform Abstract: SYNTHESIS AND BIOLOGICAL ACTIVITY OF N-SUBSTITUTED 5-FLUOROURACIL-1-ACETAMIDES. Chemischer Informationsdienst, 14 (4) doi:10.1002/chin.198304238
Veselý, Jiří, Rosenberg, Ivan, Holý, Antonín (1982) Inhibition by CTP and UTP analogues of uridine kinase from mouse leukemic cells. Collection of Czechoslovak Chemical Communications, 47. 3464-3469 doi:10.1135/cccc19823464
Holý, Antonín (1982) Stereospecific synthesis of isomeric 4-substituted 9-(2,3-dihydroxybutyl)adenines. Collection of Czechoslovak Chemical Communications, 47. 173-189 doi:10.1135/cccc19820173
 
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