Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Nicolaos Eleftheriadis"'
Autor:
Julia Stephanidou-Stephanatou, Constantinos A. Tsoleridis, Dimitra Hadjipavlou-Litina, Nicolaos Eleftheriadis, Paraskevi M. Kasapidou, Agathi Pritsa, Athanasios N. Papadopoulos, Christos A. Kontogiorgis
Publikováno v:
Synthesis. 47:1390-1398
Reaction of 3-formylchromones, 2-aminobenzimidazole, and acetonedicarboxylates under ultrasound irradiation afforded alkyl 2-(1H-benzimidazol-2-ylamino)-5-(2-hydroxyaroyl)isophthalates as the only reaction product in almost quantitative yields. Howev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff9e0add4ea21ed0a9ae2b7b84c23249
https://doi.org/10.1055/s-0034-1380154
https://doi.org/10.1055/s-0034-1380154
Autor:
Constantinos A. Tsoleridis, Constantinos G. Neochoritis, Nicolaos Eleftheriadis, Julia Stephanidou-Stephanatou, Arianna Tsiantou
Publikováno v:
Synlett. 24:2768-2772
The potential hydroacridinone synthesis using simple and inexpensive starting materials, namely 1,3-dicarbonyl compounds, anilines, formaldehyde and DBU as a stoichiometric base was explored. As a result, from the reaction of 1,3-cyclohexanedione and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9f3f99eedd313a143262ee73ffd7150
https://doi.org/10.1055/s-0033-1339922
https://doi.org/10.1055/s-0033-1339922
Autor:
Julia Stephanidou-Stephanatou, Nicolaos Eleftheriadis, Constantinos G. Neochoritis, Constantinos A. Tsoleridis
Publikováno v:
Tetrahedron. 66:709-714
Upon reaction of 1-arylamino-imidazole-2-thiones 1 with dimethyl acetylenedicarboxylate (DMAD) in the presence of 2.2 equiv of sodium hydride, imidazothiazoles 4 were exclusively formed (71–82% yield). However, from the reaction of 1 with DMAD in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b401bc265d2d12c81a582fcd8e65d65
https://doi.org/10.1016/j.tet.2009.11.056
https://doi.org/10.1016/j.tet.2009.11.056
Autor:
Athanasios N. Papadopoulos, Constantinos A. Tsoleridis, Christos A. Kontogiorgis, Nicolaos Eleftheriadis, Agathi Pritsa, Dimitra Hadjipavlou-Litina, Julia Stephanidou-Stephanatou, Paraskevi M. Kasapidou
Publikováno v:
ChemInform. 46
Starting from 3-formylchromones, acetonedicarboxylates and 2-aminobenzimidazole or aryl amines an efficient one-step method to new hydroxyaroylbenzimidazole or hydroxyaroylpyridinecarboxylate derivatives, respectively, is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::526176e197cae703cfbc64c827d7d30e
https://doi.org/10.1002/chin.201538147
https://doi.org/10.1002/chin.201538147
Autor:
Nicolaos Eleftheriadis, Arianna Tsiantou, Constantinos G. Neochoritis, Julia Stephanidou-Stephanatou, Constantinos A. Tsoleridis
Publikováno v:
ChemInform. 45
The potential hydroacridinone synthesis using simple and inexpensive starting materials, namely 1,3-dicarbonyl compounds, anilines, formaldehyde and DBU as a stoichiometric base was explored. As a result, from the reaction of 1,3-cyclohexanedione and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aece9f618634b66d5426987675ff12be
https://doi.org/10.1002/chin.201417166
https://doi.org/10.1002/chin.201417166
Autor:
Nicolaos Eleftheriadis, Zafiroula Iakovidou-Kritsi, Constantinos A. Tsoleridis, Julia Stephanidou-Stephanatou, Constantinos G. Neochoritis
Publikováno v:
ChemInform. 45
The synthesis of the title compounds and the evaluation of their in vitro cytogenic activity at typical concentration rates of the drug 1,4-benzodiazepine is presented.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c8ce1c37962ce009f92387c0ee296a69
https://doi.org/10.1002/chin.201405173
https://doi.org/10.1002/chin.201405173
Autor:
Constantinos A. Tsoleridis, Constantinos G. Neochoritis, Julia Stephanidou-Stephanatou, Nicolaos Eleftheriadis, Zafiroula Iakovidou-Kritsi
Publikováno v:
European journal of medicinal chemistry. 67
1,5-Benzo-, naphtho-, and pyridodiazepines 3 have been synthesized in excellent yields in one-step from the reaction of o-phenylenediamines with acetonedicarboxylates through microwave assisted acid catalysis. In order to ascertain their cytogenetic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18f1a760162fa1d3fb6b1fe81044a1c4
https://pubmed.ncbi.nlm.nih.gov/23871910
https://pubmed.ncbi.nlm.nih.gov/23871910