Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Iveta Wiedermannová"'
Publikováno v:
ARKIVOC, Vol 2003, Iss 15, Pp 65-74 (2003)
Externí odkaz:
https://doaj.org/article/69817cae06544919907c666c6d94362b
Publikováno v:
ARKIVOC, Vol 2003, Iss 1, Pp 22-28 (2003)
Externí odkaz:
https://doaj.org/article/782126ba99f344a9beddd9896f1f2ff9
Publikováno v:
ResearcherID
Scopus-Elsevier
Scopus-Elsevier
As known, some derivatives of quinolin-4(1H)-one possess interesting biological properties. The biological and cytostactic activity of 2-substituted 3-hydroxyquinolin-4(1H)-ones has not been reported yet. In this paper the synthesis of a series of ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::850b22c72a43419f91142f8659a13682
https://doi.org/10.1002/jhet.5570410311
https://doi.org/10.1002/jhet.5570410311
Publikováno v:
Scopus-Elsevier
ARKIVOC, Vol 2003, Iss 15, Pp 65-74 (2003)
ARKIVOC, Vol 2003, Iss 15, Pp 65-74 (2003)
3-(4-Aminophenyl)-1,2-dihydro-quinoxaline-2-one (2b), 3-(2-aminophenyl)-6,7-dimethyl-1,2dihydro-quinoxaline-2-one (1b), its 3-(4-aminophenyl)-isomer (3b), 3-(2-aminobenzyl)-1,2dihydro-quinoxaline-2-one (4b), its 3-(4-aminobenzyl)-isomer (6b), 3-(2-am
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28d869645596eac01bbdadddcef0341c
https://doi.org/10.3998/ark.5550190.0004.f08
https://doi.org/10.3998/ark.5550190.0004.f08
Publikováno v:
Journal of Heterocyclic Chemistry. 40:805-811
A series of 6-azacytosines 4a-4k and 5a-5c were prepared by nucleophilic cleavage of furan ring of [1]benzofuro[2,3-e][1,2,4]triazine derivative 1. Some of them were used for the preparation of derivatives of [1,2,4]triazolo[4,3-d][1,2,4]triazine (6a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32d4083b585182c5a0ae0446ff1b6d8e
https://doi.org/10.1002/jhet.5570400509
https://doi.org/10.1002/jhet.5570400509
Publikováno v:
ARKIVOC, Vol 2003, Iss 1, Pp 22-28 (2003)
Lamotrigine oxoanalog 8 was prepared using 5-(2-amino-5,6-dichlorophenyl)-6-azauracil 3 as starting compound. A series of 5-(2,3-dichlorophenyl)-6-azauracil derivatives 9–12 with additional substituents in the benzene ring were synthesized as well.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f055ea00f060ef5f14f316a10d31fd3
https://doi.org/10.3998/ark.5550190.0004.103
https://doi.org/10.3998/ark.5550190.0004.103
Autor:
Iveta Wiedermannová, Petr Bednář, Petr Barták, Karel Lemr, Jan Hlaváč, Juraj Ševčík, Jakub Stýskala, Zdeněk Stránský
Publikováno v:
Journal of Mass Spectrometry. 37:1213-1218
A method based on the coupling of capillary electrophoresis with mass spectrometry (CE/MS) was developed for the monitoring of 3-quinuclidinol and its four N-alkyl derivatives (methyl, ethyl, propyl and isopropyl derivatives). A fragmentation study (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e48097f74c26db406d0c5d4ac50dbd42
https://doi.org/10.1002/jms.380
https://doi.org/10.1002/jms.380
Autor:
Jan Slouka, Iveta Wiedermannová
Publikováno v:
Journal of Heterocyclic Chemistry. 38:1465-1468
By diazotization of 3-(2-aminophenyl)-1,2-dihydroquinoxaline 1c, its 3-(4-aminophenyl)-isomer2c, 3-(2-aminobenzyl)-1,2-dihydroquinoxaline-2-one 3c and its 3-(4-aminobenzyl)-isomer 4c and by azo coupling of formed diazonium salts with ethyl cyanoacety
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2af4764d22104794962cb0ee47799691
https://doi.org/10.1002/jhet.5570380633
https://doi.org/10.1002/jhet.5570380633
Autor:
Iveta Wiedermannová, Jan Slouka
Publikováno v:
ChemInform. 33
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ca712cf3209b71ce3b0624d006daf22
https://doi.org/10.1002/chin.200217159
https://doi.org/10.1002/chin.200217159
Publikováno v:
ChemInform. 35
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ff2a079f7b847a500be4660ad02c899
https://doi.org/10.1002/chin.200411148
https://doi.org/10.1002/chin.200411148