Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Linda Supe"'
Autor:
Linda Supe
Publikováno v:
Medical Sciences Forum, Vol 14, Iss 1, p 23 (2022)
Beta-amino alcohols are versatile chemicals used as scaffolds in medicinal chemistry and they are key factors for the efficacy of numerous pharmaceutical products. Locking the conformation of the active fragment in bioactive molecules may increase th
Externí odkaz:
https://doaj.org/article/6303e1fff8814e90abb3ad538f1440a9
Autor:
Mostafa Kiamehr, Firouz Matloubi Moghaddam, Satenik Mkrtchyan, Volodymyr Semeniuchenko, Linda Supe, Alexander Villinger, Peter Langer, Viktor O. Iaroshenko
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 1119-1126 (2013)
The cyclization of cyclohexane-1,3-diones with various substituted pyridinium salts afforded functionalized 8-oxa-10-aza-tricyclo[7.3.1.02,7]trideca-2(7),11-dienes. The reaction proceeds by regioselective attack of the central carbon atom of the 1,3-
Externí odkaz:
https://doaj.org/article/009419a2c8824294b6fef0d2caf63b4a
Autor:
Syeda Abida Ejaz, Jamshed Iqbal, Saira Afzal, Joanna Lecka, Alexander Villinger, Peter Langer, Jean Sévigny, Martin Hein, Abid Mahmood, Viktor O. Iaroshenko, Linda Supe
Publikováno v:
European Journal of Organic Chemistry. 2018:2629-2644
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4caa1640b6a2a4631a35e0eda083c3b0
https://doi.org/10.1002/ejoc.201800163
https://doi.org/10.1002/ejoc.201800163
Publikováno v:
Tetrahedron. 76:131522
A number of new fluorinated and non-fluorinated glycosides of 1H-pyrazolo[3,4-b]pyridin-3(2H)-ones were synthesized by direct attachment of the carbohydrate moiety to the heterocycle using the silyl Hilbert-Jones glycosylation method. The products we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4cda9ce29dccdfd6b79a62252fdf9f8d
https://doi.org/10.1016/j.tet.2020.131522
https://doi.org/10.1016/j.tet.2020.131522
Autor:
Andrei A. Tolmachev, Satenik Mkrtchyan, Muhammad S. A. Abbasi, Ani Hakobyan, Alexander Villinger, Dmitriy M. Volochnyuk, Linda Supe, Ashot Gevorgyan, Dmytro Ostrovskyi, Knar Arakelyan, Marcelo Vilches-Herrera, Viktor O. Iaroshenko
Publikováno v:
Tetrahedron. 69:1217-1228
The synthesis of 1-deazapurines and isosteres bearing the exocyclic nitrogen atom at position-1 was developed basing on the formal [3+3]-cyclization reaction of nitro-malonaldehyde with the set of electron-excessive aminoheterocycles. Through the fun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::918ad3b3483e1d0362d6caf455e56b63
https://doi.org/10.1016/j.tet.2012.11.026
https://doi.org/10.1016/j.tet.2012.11.026
Autor:
Aneela Maalik, Linda Supe, Andrei A. Tolmachev, Peter Langer, Vyacheslav Ya. Sosnovskikh, Ani Hakobyan, Viktor O. Iaroshenko, Satenik Mkrtchyan, Alexander Villinger, Gagik Ghazaryan, Dmytro Ostrovskyi, Tariel V. Ghochikyan
Publikováno v:
Synthesis. 2011:469-479
The first synthesis of 3-(dichloroacetyl)chromone from 3-(dimethylamino)-1-(2-hydroxyphenyl)propen-1-one and dichlo- roacetyl chloride is described. The reaction of electron-rich amino- heterocycles with 3-(dichloroacetyl)chromone provides a set of d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56abfffba6f26441a4f96bf5b1b933c6
https://doi.org/10.1055/s-0030-1258364
https://doi.org/10.1055/s-0030-1258364
Autor:
Peter Langer, Alexander Villinger, Firouz Matloubi Moghaddam, Viktor O. Iaroshenko, Volodymyr Semeniuchenko, Mostafa Kiamehr, Linda Supe, Satenik Mkrtchyan
Publikováno v:
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 1119-1126 (2013)
Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 1119-1126 (2013)
The cyclization of cyclohexane-1,3-diones with various substituted pyridinium salts afforded functionalized 8-oxa-10-aza-tricyclo[7.3.1.02,7]trideca-2(7),11-dienes. The reaction proceeds by regioselective attack of the central carbon atom of the 1,3-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::529838090e3fc81daa8c65d911a66bc8
https://pubmed.ncbi.nlm.nih.gov/23843903
https://pubmed.ncbi.nlm.nih.gov/23843903
Autor:
Linda Supe, Maria Milyutina, Alina Bunescu, Viktor O. Iaroshenko, Anke Spannenberg, Peter Langer
Publikováno v:
ChemInform. 43
Treatment of bis-silyl enol ethers (II) with chromones (I) affords a variety of functionalized dihydroxybenzophenones (III).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::46ae866f928292bfce262ba68ec73c16
https://doi.org/10.1002/chin.201217087
https://doi.org/10.1002/chin.201217087
Autor:
Anke Spannenberg, Maria Milyutina, Alina Bunescu, Linda Supe, Viktor O. Iaroshenko, Peter Langer
Publikováno v:
Organic & Biomolecular Chemistry. 9:7554
The reaction of 1,3-bis-silyl enol ethers with 3-methoxalylchromones affords a great variety of functionalised 2,4'-dihydroxybenzophenones. These products are formed by a domino Michael/retro-Michael/Mukaiyama-aldol reaction. The synthesized compound
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::358522bce505bcd555f7fb476f65bc30
https://doi.org/10.1039/c1ob05931a
https://doi.org/10.1039/c1ob05931a