Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Gábor Varró"'
Publikováno v:
Periodica Polytechnica Chemical Engineering. 67:31-40
An efficient stereoselective synthesis of a pivotal intermediate, a cyclic allyl alcohol derivative containing two methoxy groups [(±)-22], using for the preparation of (±)-trans-dihydronarciclasine analogues was elaborated starting from easily ava
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ff2487d9703500c3f3b9a296a0d9104
https://doi.org/10.3311/ppch.20438
https://doi.org/10.3311/ppch.20438
Autor:
György Szabó, Olivér Éliás, Péter Erdélyi, Attila Potor, György I. Túrós, Benedek I. Károlyi, Gábor Varró, Ágnes Gy. Vaskó, Imre Bata, Gábor L. Kapus, Zoltán Dohányos, Amrita Á. Bobok, László Fodor, Márta Thán, Mónika Vastag, Zsolt Komlódi, Rita É. Soukupné Kedves, Éva Makó, Brigitta Süveges, István Greiner
Publikováno v:
Journal of Medicinal Chemistry. 65:7876-7895
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::12781b28dd2ce761e3b095ba5fa57f9a
https://doi.org/10.1021/acs.jmedchem.2c00414
https://doi.org/10.1021/acs.jmedchem.2c00414
Autor:
György, Szabó, Olivér, Éliás, Péter, Erdélyi, Attila, Potor, György I, Túrós, Benedek I, Károlyi, Gábor, Varró, Ágnes Gy, Vaskó, Imre, Bata, Gábor L, Kapus, Zoltán, Dohányos, Amrita Á, Bobok, László, Fodor, Márta, Thán, Mónika, Vastag, Zsolt, Komlódi, Rita É, Soukupné Kedves, Éva, Makó, Brigitta, Süveges, István, Greiner
Publikováno v:
Journal of medicinal chemistry. 65(11)
The discovery and characterization of novel naphthyridine derivatives with selective α5-GABA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::822b13f51a6ed446d107716a3b87677b
https://pubmed.ncbi.nlm.nih.gov/35584373
https://pubmed.ncbi.nlm.nih.gov/35584373
Publikováno v:
Synthesis. 50:625-643
Several new trans-dihydronarciclasine analogues were stereoselectively synthesised by applying our feasible and efficient process developed recently. These new phenanthridone alkaloid derivatives were obtained in both racemic and optically active f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::13d39cb51959af11c43d982e029a06e1
https://doi.org/10.1055/s-0036-1591514
https://doi.org/10.1055/s-0036-1591514
Publikováno v:
European journal of medicinal chemistry. 173
A series of (±)-trans-dihydronarciclasine and (±)-trans-dihydrolycoricidine derivatives with variously substituted ring A was synthesised and evaluated for their antiproliferative activity against 60 human tumour cell lines (NCI60), representing le
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d451a1b8e93b6a64f377f23818bdbc5c
https://pubmed.ncbi.nlm.nih.gov/30986573
https://pubmed.ncbi.nlm.nih.gov/30986573
Publikováno v:
Monatshefte Fur Chemie
Some new trans-dihydronarciclasine derivatives containing a 1,4-benzodioxane moiety were stereoselectively synthesised using our feasible and efficient method developed recently. These new phenanthridone alkaloid analogues were obtained in both racem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84d56617eb08b651c5ad56bf0cadd418
https://pubmed.ncbi.nlm.nih.gov/32214482
https://pubmed.ncbi.nlm.nih.gov/32214482
Publikováno v:
Tetrahedron Letters. 57:1544-1546
A short and efficient stereoselective total synthesis of (±)-trans-dihydronarciclasine (1), a highly potent naturally occurring antineoplastic agent, was developed from readily available vanillin (7). The key intermediate of this new synthesis was a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b74bad154f88d45261c46bcc62ea8c4e
https://doi.org/10.1016/j.tetlet.2016.02.089
https://doi.org/10.1016/j.tetlet.2016.02.089
Autor:
Alajos Grün, László Hegedűs, András Simon, István Kádas, Ibolya Leveles, Beáta G. Vértessy, Attila Balogh, Gábor Varró
Publikováno v:
Journal of natural products. 80(6)
A feasible and enantioselective total synthesis of (−)-trans-dihydronarciclasine [(−)-1], a highly biologically active alkaloid, was devised starting from vanillin (8). The key step of this new synthesis was an asymmetric, organocatalytic Michael
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b43e64813f7288f030a423179ffe7633
https://pubmed.ncbi.nlm.nih.gov/28581297
https://pubmed.ncbi.nlm.nih.gov/28581297