Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Kangah Niameke Jean-Baptiste"'
Autor:
Ballo Daouda, Nanou Tiéba Tuo, Tuncer Hökelek, Kangah Niameke Jean-Baptiste, Kodjo Charles Guillaume, Kablan Ahmont Landry Claude, El Mokhtar Essassi
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 76, Iss 5, Pp 605-610 (2020)
The title compound, C18H16N2O2, consists of perimidine and methoxyphenol units, where the tricyclic perimidine unit contains a naphthalene ring system and a non-planar C4N2 ring adopting an envelope conformation with the NCN group hinged by 47.44 (7)
Externí odkaz:
https://doaj.org/article/b8d16b97bc8e44c48dd1f76ac9b95cc7
Autor:
Ballo Daouda, Yapo Ossey Bernard, Pacôme Kouadio N’Go, Kodjo Charles Guillaume, Tuo Nanou Tiéba, Ziao Nahossé, Kangah Niameke Jean Baptiste
Publikováno v:
Journal of Pharmaceutical Research International. :52-60
Background and Aim: The 1H-perimidne, as novel source carbene ligand, is well known for its anti-fungal, anti-microbial or anti-tumor activities. Here, we aimed to study the acute toxicity in Wistar rat of 2-(2,3-dihydro-1H-perimidin-2-yl)-6-methoxyp
Autor:
Kodjo Charles Guillaume, Tuo Nanou Tiéba, Yapo Ossey Bernard, Kangah Niameke Jean Baptiste, Ballo Daouda, Kablan Ahmont Landry Claude, Ziao Nahossé
Publikováno v:
Journal of Biophysical Chemistry. 12:1-9
From (2,3-dihydro-1H-perimidin-2-yl)-phenyl, the substitution of OH group in ortho or para position on the phenyl ring, allows us to synthesize the studied compounds. These three compounds have been characterized by conventional spectroscopic methods
Autor:
TUO, Nanou Tiéba, KANGAH, Niameke Jean Baptiste, BALLO, Daouda, SANHOUN, Aimé R., Kablan, Ahmont Landry Claude, KODJO, Charles Guillaume, YAPO, Ossey Bernard, ZIAO, Nahossé
We report here the synthesis, characterization and antimicrobial activity of three molecules from the family of 2,3-dihydro -1H-perimidines derived from 1,8-diaminonaphthalene. The three perimidines were characterized by conventional spectrometry met
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4bcec3da934d177dd7a71a1c9ea39ec0
Autor:
Ballo, Daouda, Nanou Tiéba, Tuo, Tuncer, Hökelek, Kangah, Niameke Jean-Baptiste, Kodjo, Charles Guillaume, Kablan Ahmont Landry, Claude, El Mokhtar, Essassi
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications
The title compound consists of perimidin and methoxyphenol units. In the crystal, O—HPhnl⋯NPrmdn and N—HPrmdn⋯OPhnl (Phnl = phenol and Prmdn = perimidine) hydrogen bonds link the molecules into infinite chains along the b-axis direction
Autor:
Daouda, Ballo, Nanou Tiéba Tuo, Kangah, Niameke Jean-Baptiste, Hökelek, Tuncer, Kodjo, Charles Guillaume, Retailleau, Pascal, Essassi, El Mokhtar
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications; Jun2020, Vol. 76 Issue 6, p798-802, 12p
Autor:
Kangah Niameke Jean-Baptiste, Dibi Konan Jacques, Kodjo Charles Guillaume, Kablan Ahmont Landry Claude, Ouattara Zana Adama, Ziao Nahossé, Kouame Bosson Antoine
Publikováno v:
IRA-International Journal of Applied Sciences (ISSN 2455-4499). 7:69
We report herein synthesis, characterization and antimicrobial activity of four Shiff bases derived from hexamethylenediamine. Substitution of a nitro group on each aromatic ring in ortho, meta or para positions of N,N'-bis(phenylmethyl)hexane-1,6-di
Autor:
Kablan Ahmont Landry Claude, Kangah Niameke Jean-Baptiste, Ziao Nahossé, Angora Rémi Constant Ahoua, Koné Mamidou Witabouna, Kodjo Charles Guillaume
Publikováno v:
IRA-International Journal of Applied Sciences (ISSN 2455-4499). 6:23
From N,N'-bis(phenylmethylene)cyclohexane-1,2-diamine, substitution of a nitro group on each aromatic ring and its systematic displacement in the positions ortho, meta and para positions allowed to synthesize a homogeneous series of positional isomer
Autor:
Daouda B; Laboratoire de Chimie Organique Heterocyclique URAC 21, Pôle de Competence Pharmacochimie, Faculté des Sciences, Université Mohammed V, Rabat, Morocco.; Laboratoire de Chimie Organique et de Substances Naturelles, UFR Sciences des Structures de la Matière et Technologie, Université Félix Houphouët-Boigny, 22 BP 582 Abidjan, Côte d'Ivoire., Tuo NT; Laboratoire de Thermodynamique et Physicochimie du Milieu, Université Nangui, Abrogoua, UFR-SFA, 02 BP 801 Abidjan 02, Côte d'Ivoire., Kangah NJ; Laboratoire de Thermodynamique et Physicochimie du Milieu, Université Nangui, Abrogoua, UFR-SFA, 02 BP 801 Abidjan 02, Côte d'Ivoire., Hökelek T; Department of Physics, Hacettepe University, 06800 Beytepe, Ankara, Turkey., Kodjo CG; Laboratoire de Thermodynamique et Physicochimie du Milieu, Université Nangui, Abrogoua, UFR-SFA, 02 BP 801 Abidjan 02, Côte d'Ivoire., Retailleau P; Institut de Chimie des Substances Naturelles, 1 av. de la Terrasse, 91198 Gif sur Yvette, France., Essassi EM; Laboratoire de Chimie Organique Heterocyclique URAC 21, Pôle de Competence Pharmacochimie, Faculté des Sciences, Université Mohammed V, Rabat, Morocco.
Publikováno v:
Acta crystallographica. Section E, Crystallographic communications [Acta Crystallogr E Crystallogr Commun] 2020 May 05; Vol. 76 (Pt 6), pp. 798-802. Date of Electronic Publication: 2020 May 05 (Print Publication: 2020).