Zobrazeno 1 - 10
of 219
pro vyhledávání: '"Tamás Patonay"'
Publikováno v:
ARKIVOC, Vol 2012, Iss 5, Pp 210-225 (2012)
Externí odkaz:
https://doaj.org/article/552a643065064831aaa92b02b69e6b6c
Publikováno v:
ARKIVOC, Vol 2004, Iss 7, Pp 183-195 (2004)
Externí odkaz:
https://doaj.org/article/0dca410955cf4fa6b95c84d06f8d1ac3
Publikováno v:
ARKIVOC, Vol 2004, Iss 7, Pp 106-123 (2004)
Externí odkaz:
https://doaj.org/article/e214ff7edb0c4467a512f12e4708bfea
Publikováno v:
ARKIVOC, Vol 2001, Iss 3, Pp 40-50 (2002)
Externí odkaz:
https://doaj.org/article/41321f9a7bf74015a7d9d35f9470115b
Autor:
Sylvestre Bonnet, Etelka Farkas, Máté Kozsup, Péter Buglyó, Attila Cs. Bényei, Tamás Patonay, Krisztina Kónya, Xue-Quan Zhou
Publikováno v:
Journal of Inorganic Biochemistry, 217. ELSEVIER SCIENCE INC
Hypoxia activated Co(III) complexes as prodrugs may provide with a selective delivery of cytotoxic or antibacterial compounds. Whithin this field sixteen novel Co(III) ternary complexes with the general formula [Co(4N)(flav)](ClO4)2, where 4N = tris(
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1727ceae0607d45f81c797192d731a4e
https://pubmed.ncbi.nlm.nih.gov/33588278
https://pubmed.ncbi.nlm.nih.gov/33588278
Autor:
Dávid Pajtás, Zoltan Varga, Zoltán Pethő, Gyorgy Panyi, Krisztina Kónya, Tamás Patonay, Petr Džubák, Attila Kiss-Szikszai
Publikováno v:
The Journal of Organic Chemistry. 82:4578-4587
The article describes the development of Buchwald-Hartwig amination of different bromoflavones with amino acid and peptide derivatives as nitrogen source giving unique structures. The previously observed racemization, which occurred during the synthe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fd2bfdbd8917b5b572af0db525a26c1
https://doi.org/10.1021/acs.joc.7b00124
https://doi.org/10.1021/acs.joc.7b00124
Publikováno v:
Synlett. 27:2709-2715
Structurally novel carbohydrate–O-heterocycle derivatives linked by various unsaturated carbon bridges were synthesized by palladium-catalyzed cross-coupling reactions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43891f3009a03c727822596d7a4eef68
https://doi.org/10.1055/s-0036-1588591
https://doi.org/10.1055/s-0036-1588591
Publikováno v:
Synlett. 27:888-892
Structurally novel carbohydrate–flavone and –chromone derivatives with an unsaturated carbon bridge were synthesized by a phosphine-free palladium-catalyzed cross-coupling reaction.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f39b89ab370f86e2d29728a993d85f12
https://doi.org/10.1055/s-0035-1561273
https://doi.org/10.1055/s-0035-1561273
Autor:
Alexander Villinger, David Kuhrt, Marcel Sonneck, Peter Langer, Tamás Patonay, Krisztina Kónya
Publikováno v:
Synlett. 27:75-79
1,4-Diaryl-9H-fluoren-9-ones were prepared by regioselective Suzuki–Miyaura cross-coupling reaction of the bis(triflate) of 1,4-dihydroxy-9H-fluoren-9-one. The reactions proceeded with excellent site selectivity. The first attack occurs at position
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::156db03f00f9a09a04d2f52c11a1cc8c
https://doi.org/10.1055/s-0035-1560211
https://doi.org/10.1055/s-0035-1560211
Autor:
Peter Langer, Dávid Pajtás, Karoly Dihen, Alexander Villinger, Krisztina Kónya, Tamás Patonay
Publikováno v:
Synlett. 26:2601-2605
8-Aryl- and 6,8-diarylflavones were prepared by Suzuki–Miyaura reactions of 6,8-dibromoflavone. In spite of the greater steric hindrance, the first attack proceeded with good site selectivity at position 8.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::77e22cb5e01a42467b63df66e621c424
https://doi.org/10.1055/s-0035-1560633
https://doi.org/10.1055/s-0035-1560633