Zobrazeno 1 - 10
of 49
pro vyhledávání: '"Juraj Bernát"'
Autor:
Karel D. Klika, Eva Balentová, Juraj Bernát, Ján Imrich, Martina Vavrušová, Kalevi Pihlaja, Andreas Koch, Erich Kleinpeter, Alexandra Kelling, Uwe Schilde
Publikováno v:
ARKIVOC, Vol 2006, Iss 16, Pp 93-108 (2007)
Externí odkaz:
https://doaj.org/article/dacee3af548b4f7eb27853c4dacb1862
Publikováno v:
Transportation Research Procedia. 55:1563-1569
The traffic accidents between vehicles and vulnerable road users have fatal consequences in the most cases. Despite the development of active and passive vehicle safety and significant progress in the use of autonomous systems, there is still a need
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::963353082fe59d5fa2440e3dd9f46032
https://doi.org/10.1016/j.trpro.2021.07.145
https://doi.org/10.1016/j.trpro.2021.07.145
Autor:
Erich Kleinpeter, Uwe Schilde, Juraj Bernát, Andreas Koch, Alexandra Kelling, Martina Vavrušová, Eva Balentova, Ján Imrich, Karel D. Klika, Kalevi Pihlaja
Publikováno v:
ARKIVOC, Vol 2006, Iss 16, Pp 93-108 (2007)
The reaction of methyl acridin-9-ylthiosemicarbazide under basic conditions with methyl bromoacetate resulted in a 1,3-thiazolin-4-one structure as provided by X-ray crystallography. The structure forced a re-evaluation of the reactant methyl acridin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e921fa3b77d5385362101b0d1dbb6fe
https://doi.org/10.3998/ark.5550190.0007.g11
https://doi.org/10.3998/ark.5550190.0007.g11
Autor:
Erich Kleinpeter, Andreas Koch, Juraj Bernát, Karel D. Klika, Kalevi Pihlaja, Martina Vavrušová, Eva Balentova, Ján Imrich
Publikováno v:
Journal of Heterocyclic Chemistry. 43:633-643
The regioselectivities of methyl- and phenylhydrazine with acridin-9-yl isothiocyanate (thus yielding thiosemicarbazides with acridine substituted on the urea-type side) were examined. Methythydrazine regioselectivity was high with the alpha-nitrogen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4928273dea58cf6d611586cafc0ddfb
https://doi.org/10.1002/jhet.5570430317
https://doi.org/10.1002/jhet.5570430317
Publikováno v:
Journal of Heterocyclic Chemistry. 43:739-743
N-Acridin-9-yl methyl N′-acridin-9-yl thiourea spontaneously spiro cyclises via nucleophilic attack of the methylene carbon onto the C-9 of the other acridine moiety. The thiourea, upon reaction with bromoacetonitrile, provided a spiro fused-bicycl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2d8c723e17d7cf7b86127ce8ef802949
https://doi.org/10.1002/jhet.5570430331
https://doi.org/10.1002/jhet.5570430331
Autor:
Lucia Sucha, Pavol Kristian, Juraj Bernát, Kalevi Pihlaja, Mária Vilková, Ján Imrich, Eva Balentova, Karel D. Klika, Nada Prónayová
Publikováno v:
Journal of Heterocyclic Chemistry. 43:645-656
Acridin-9-yl hydrazine upon treatment with various isothiocyanates (RNCS, R = methyl, allyl, phenyl, p-methoxy phenyl, and p-nitro phenyl) yielded the corresponding thiosemicarbazides with acridine substituted on the carbazide-type side. The alkyl-su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::808681c30b4a317e28385585c0c44cb7
https://doi.org/10.1002/jhet.5570430318
https://doi.org/10.1002/jhet.5570430318
Publikováno v:
Synthetic Communications. 28:4171-4178
A convenient method has been devised for the preparation of the spirodihydro-acridinethiazolines 5a-j by the treatment of thioureas 3a-e with methyl bromoacetate and bromoacetonitrile via non-isolable isothioureas 4a-j and their subsequent cyclizatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::72fa2d773ce3834db28824d7e66f142a
https://doi.org/10.1080/00397919809458697
https://doi.org/10.1080/00397919809458697
Autor:
Gejza Suchár, Ivan Danihel, Jana Guspanová, Slávka Hočová, Ján Imrich, Anthony Linden, Tatiana Bušová, Igor Chomca, Juraj Bernát, Pavol Kristian
Publikováno v:
Molecules. 1:181-189
The specific physicochemical and spectral properties (dipole moments, NMR and fluorescence spectra) of 2- and 4-substituted 9-isothiocyanatoacridines were studied and compared with the series of m, p-substituted phenyl and benzoyl isothiocyanates. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c983adbd0354c2203d8afeeb2e3ba13d
https://doi.org/10.1007/s007830050036
https://doi.org/10.1007/s007830050036
Publikováno v:
Collection of Czechoslovak Chemical Communications. 62:1491-1496
A simple new method has been devised for the preparation of α-isothiocyanatoethers 1a-1f in good yields by reaction of PO(NCS)3 or (PhO)2PONCS with an equimolar mixture of aldehydes and alcohols. The course of nucleophilic additions of methanol, ami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cd5af4eac6c169bc85441605776991b3
https://doi.org/10.1135/cccc19971491
https://doi.org/10.1135/cccc19971491
Publikováno v:
Collection of Czechoslovak Chemical Communications. 61:432-436
Reaction of sodium salts of O-methyl-N-substituted iminothiocarbonates with bromoacetyl bromide represents a new general method for preparation of 3-substituted 1,3-thiazolidine-2,4-diones in good yields and high purity. The structure of the synthesi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8d4817ca47343427bb0fb88522af4c3
https://doi.org/10.1135/cccc19960432
https://doi.org/10.1135/cccc19960432