Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Mokhtar, Fodili"'
Autor:
Emma Bremond, Martial Boggio-Pasqua, Nadine Leygue, Mokhtar Fodili, Pascal Hoffmann, Nathalie Saffon-Merceron, Rémi Métivier, Suzanne Fery-Forgues
Publikováno v:
Dyes and Pigments
Dyes and Pigments, 2023, 211, pp.111046. ⟨10.1016/j.dyepig.2022.111046⟩
Dyes and Pigments, 2023, 211, pp.111046. ⟨10.1016/j.dyepig.2022.111046⟩
International audience; Excited-state intramolecular proton transfer (ESIPT) is a photophysical process that may lead to superior emission properties. For a long time, cinnamoyl pyrone (CP) derivatives have been classified as non-ESIPT molecules. Wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9ad40db28cc82e9195dc201cde6da41
https://hal.science/hal-03934075/document
https://hal.science/hal-03934075/document
Autor:
Hebbache, Zahida Yasmina, Yazid, Foudil-Cherif, Mohammedi, Hichem, Belfadel, Ouahiba, Mokhtar, Fodili
Publikováno v:
Carpathian Journal of Food Science & Technology; 2021, Vol. 13 Issue 3, p158-172, 15p
Autor:
Christian Lherbet, Mohamed Amari, Beatrice Silvia Orena, Frédéric Rodriguez, Mokhtar Fodili, Nadji Belkheiri, Bachar Rébat Moulkrere, Nathalie Saffon-Merceron, Giorgia Mori, Pascal Hoffmann
Publikováno v:
Medicinal Chemistry Research
Medicinal Chemistry Research, Springer Verlag, 2018, 27 (1), pp.308-320. ⟨10.1007/s00044-017-2064-x⟩
Medicinal Chemistry Research, Springer Verlag, 2018, 27 (1), pp.308-320. ⟨10.1007/s00044-017-2064-x⟩
Two series of heterocyclic compounds derived from 3-acetyl-4-hydroxy-6-methyl-2H-pyran-2-one (DHA) and 2-acetylbutyrolactone have been synthesized and characterized. The compounds were evaluated for their activities against Mycobacterium tuberculosis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fcd46bd568cc6ae5810535e6f3b3fdb
https://hal.archives-ouvertes.fr/hal-02058656
https://hal.archives-ouvertes.fr/hal-02058656
Autor:
Nathalie Saffon-Merceron, Christian Lherbet, Marc Vedrenne, Bellara Nedjar-Kolli, Mokhtar Fodili, Pascal Hoffmann
Publikováno v:
Chemistry of Heterocyclic Compounds
Chemistry of Heterocyclic Compounds, Springer Verlag, 2015, 51 (10), pp.940-943. ⟨10.1007/s10593-015-1801-7⟩
Chemistry of Heterocyclic Compounds, Springer Verlag, 2015, 51 (10), pp.940-943. ⟨10.1007/s10593-015-1801-7⟩
The synthesis of an 1,4-disubstituted 5-methylimidazole is reported by reacting toluenesulfonylmethyl isocyanide with an enaminic tautomeric form of a secondary ketimine in the presence of catalytic amounts of bismuth(III) triflate. A possible mechan
Autor:
Christian Lherbet, Pascal Hoffmann, Marc Vedrenne, Nathalie Saffon-Merceron, Bellara Nedjar-Kolli, Mokhtar Fodili
Publikováno v:
ChemInform. 47
The synthesis of an 1,4-disubstituted 5-methylimidazole is reported by reacting toluenesulfonylmethyl isocyanide with an enaminic tautomeric form of a secondary ketimine in the presence of catalytic amounts of bismuth(III) triflate. A possible mechan
Autor:
Pascal Hoffmann, Omar Bouaziz, Mokhtar Fodili, Mohamed Amari, Nawal Bayou-Khier, Fairouz Abboub
Publikováno v:
Comptes Rendus Chimie. 15:774-778
Resume Quelques derives originaux de structure 1,5-benzodiazepine 4 ont ete obtenus par reaction de l’acide dehydroacetique (DHA) hydrogene en C 5 -C 6 avec des orthophenylenediamines et des aldehydes aromatiques. L’interpretation des resultats o
Publikováno v:
Letters in Organic Chemistry. 6:354-358
The preparation of a series of 1,5-disubstituted-4-methyl imidazoles is reported, based on an unprecedented re- action between an acetimine and TosMIC in the presence of tert-butylamine and catalytic amounts of bismuth(III) triflate. The mechanism is
Autor:
Rebat Bachar, Mokhtar Fodili, Mohamed Amari, Filipe A. Almeida Paz, Nawal Bayou Khier, Oualid Talhi, Artur M. S. Silva, Omar Bouaziz
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
A two-step procedure transformation starting from the reaction of ortho-phenylenediamines on 2-acetylbutyrolactone 1 yielded (Z)-3-(1-aminoethylidene)butyrolactones 2, which were treated with either N,N-dimethylformamide dimethyl acetal, triphosgene,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12af38fa649f772026e0e9c43f987c6c
http://hdl.handle.net/10773/19767
http://hdl.handle.net/10773/19767
Publikováno v:
Journal of Heterocyclic Chemistry. 39:811-816
Reaction of pyrone 1a or tetronic acid 1b with o-phenylenediamine derivatives gave enaminone compounds 2. When reacting with different electrophiles, these intermediates allowed versatile access to different heterocyclic structures: when DMA derivati
Publikováno v:
ChemInform. 33