Zobrazeno 1 - 7
of 7
pro vyhledávání: '"ABLO, Evrard"'
Autor:
Ablo, Evrard1 (AUTHOR), Coulibaly, Souleymane1 (AUTHOR) souleydestras@yahoo.fr, Coulibali, Siomenan1 (AUTHOR) siomenan.coulibaly76@ufhb.edu.ci, Signo, Kouassi2 (AUTHOR), Achi, Patrick‐Armand1 (AUTHOR), Giraud, Nicolas3 (AUTHOR), Bertho, Gildas3 (AUTHOR) gildas.bertho@u-paris.fr
Publikováno v:
Magnetic Resonance in Chemistry. Dec2022, Vol. 60 Issue 12, p1157-1170. 14p.
Autor:
Ablo, Evrard1 (AUTHOR), Coulibali, Siomenan1 (AUTHOR), Touré, Daouda2 (AUTHOR), Coulibaly, Souleymane1 (AUTHOR), Kablan, Ahmont Landry Claude2 (AUTHOR), Konan Kouadio, Fernique3 (AUTHOR), Sissouma, Drissa1 (AUTHOR), Guessend Kouadio, Nathalie3 (AUTHOR), Ané, Adjou1 (AUTHOR)
Publikováno v:
Synthetic Communications. 2022, Vol. 52 Issue 3, p462-469. 8p. 3 Diagrams, 2 Charts.
Autor:
ACHI, Armand Patrick, Doumadé ZON, Adéyolé TIMOTOU, ABLO, Evrard, KABLAN, Claude Landry Ahmont, Siomenan COULIBALI
Publikováno v:
GSC Advanced Research and Reviews. 12:018-025
The present work highlights the synthesis and effect of introducing substituents on the nitrogen at position -1 of five 2-benzylthiopyrimidine derivatives (6a-e). The compounds (6a-e) were obtained by condensation of 2-thiopyrimidines (4) with benzyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::141c2b97926fef3efeb8074c8f067a4e
https://doi.org/10.30574/gscarr.2022.12.3.0230
https://doi.org/10.30574/gscarr.2022.12.3.0230
Autor:
ABLO, Evrard, Sioménan COULIBALI, Tchambaga Etienne CAMARA, Bakary COULIBALY, Doumadé ZON, ACHI, Patrick Armand, Ané ADJOU
To explore the antibacterial activity, a series of new 2-thioalkyl-3-nitroimidazo[1,2-a]pyridine derivatives (5a-k) were synthesized and characterized by 1H, 13C Nuclear Magnetic Resonance (NMR), and High-Resolution Mass Spectrometry (HRMS) analyses.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d366f01172bbda513c08f1231bb4c5e8
Autor:
null Souleymane Coulibaly, null Sioménan Coulibali, null Fanté Bamba, null Patrick-Armand Achi, null Fernique Konan Kouadio, null Ablo Evrard, null Adjou Ané
In pursuit the development of novel potent and selective antibacterial agents, we synthesized twelve (12) N-alkyl 2-benzylthiomethyl-1H-benzimidazole derivatives and evaluated their antibacterial activities. Their antibacterial profile was determined
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39b3f19c599c2262c7cb1e163d58be7c
Autor:
null Ablo Evrard, null Souleymane Coulibaly, null Siomenan Coulibali, null Kouassi Signo, null Patrick‐Armand Achi, null Nicolas Giraud, null Gildas Bertho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5200cf770199e3754bd29357d1647b8c
https://doi.org/10.1002/mrc.5308/v3/response1
https://doi.org/10.1002/mrc.5308/v3/response1
Autor:
Toure Daouda, Sissouma Drissa, Ablo Evrard, Adjou Ané, Coulibaly Souleymane, Coulibali Siomenan, Camara Tchambaga Etienne
Publikováno v:
Advances in Biological Chemistry. 11:165-177
A series of novel substituted benzimidazole (7a - n) derivatives were synthesized and characterized by 1H, 13C Nuclear Magnetic Resonance (NMR) spectra and High Resolution Mass Spectrometry (HRMS). The substitution was done in position -1 and -2 by a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c446ff6bfb4c4a1b5135787b129a90d4
https://doi.org/10.4236/abc.2021.114012
https://doi.org/10.4236/abc.2021.114012