Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Venance Martial, Say"'
Autor:
Venance Martial Say, Philippe M. Loiseau, Pierre Champy, Faustin Aka Kabran, Laurent Evanno, Bruno Figadère, Timothée Aboua Okpekon, Alexandre Maciuk
Publikováno v:
Natural Product Research. 35:5112-5119
Bioassay guided fractionation of the stem barks of Isolona cooperi led to the isolation of a new lactone, apoprunellelactone (APL, 1), and two known compounds, 5-[1-hydroxyhexyl]-2H-furan-2-one (2) and oleic acid (3). Their structures were elucidated
Autor:
Timothée Aboua, Okpekon, Faustin Aka, Kabran, Venance Martial, Say, Laurent, Evanno, Alexandre, Maciuk, Philippe, Loiseau, Pierre, Champy, Bruno, Figadère
Publikováno v:
Natural product research. 35(23)
Bioassay guided fractionation of the stem barks of
Publikováno v:
International Journal of Biological and Chemical Sciences; Vol 13, No 3 (2019); 1826-1836
Five symmetrical near infrared dyes having different linker between the two heterocycles were synthesized by condensation of N-alkylbenzo[c,d]indolium salts with either squaric acid or imine. All synthesized dyes showed strong absorbance in the near-
Autor:
Ané Adjou, Venance Martial Say, Roger Simplice Pépin Zoakouma, Sagne Jacques Akpa, Drissa Sissouma, Siomenan Coulbali, Fante Bamba
Publikováno v:
International Journal of Biological and Chemical Sciences; Vol 11, No 3 (2017); 1320-1335
For the synthesis of novel thiazolo[3,2-a]benzimidazol-3-ones and thiazolo[3,2-a]benzimidazoles, two methods have been developed which afforded the target compounds in relatively good yields by a pot process. The reaction between 2-mercapto-1H-benzim
Autor:
Drissa Sissouma, Venance Martial Say, Mamidou Witabouna Kone, Mahama Ouattara, Sagne Jacques Akpa, Ané Adjou, Roger Simplice Pépin Zoakouma
Publikováno v:
International Journal of Biological and Chemical Sciences. 10:1403
The aim of this study is to find potent biomolecules against infectious germs. Based on the reactivity of some key positions of the benzimidazole core, the first part of this work consisted of the synthesis of a series of substituted 2-thioalkylaryl-