Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ayoub El mahmoudi"'
Publikováno v:
Molbank, Vol 2023, Iss 3, p M1678 (2023)
In this work, a new compound, 2-(N-allylsulfamoyl)-N-propylbenzamide, has been synthesized via a tandem one-pot reaction under sonication. The rotational orientations of the allylsulfamoyl and the amide groups in the title molecule, C13H18N2O3S, are
Externí odkaz:
https://doaj.org/article/8d4a54acfef947bca1ee7523ab5009e9
Publikováno v:
Molbank, Vol 2022, Iss 4, p M1529 (2022)
In this work, we present an efficient one-pot method for the synthesis of three new azo-isoxazoline derivatives (4a–c) from aromatic aldehydes, hydroxylamine hydrochloride and 4-(allyloxy)azobenzene. Thus, the azo-isoxazoline derivatives (4a–c) w
Externí odkaz:
https://doaj.org/article/ef16cec4b47a449e80df200072c0ad77
Publikováno v:
Molbank, Vol 2022, Iss 4, p M1488 (2022)
In this work, a novel compound N-(3-(4-methoxyphenyl)isoxazolin-5-yl)methylsaccharin has been synthesized. The molecular structure of the compound was determined using various spectroscopic techniques and confirmed by a single-crystal X-ray diffracti
Externí odkaz:
https://doaj.org/article/583c5fd4178e486e9e31675fb0556059
Autor:
Ayoub El Mahmoudi, Hind El Masaoudi, Hamza Tachallait, Aicha Talha, Suhana Arshad, Rachid Benhida, Boujemaâ Jaber, Mohammed Benaissa, Khalid Bougrin
Publikováno v:
Results in Chemistry, Vol 4, Iss , Pp 100552- (2022)
The Ag3PO4-MEA catalyst was successfully prepared and proved to be an efficient and selective catalyst of the multicomponent synthesis of a new library of 1,4-disubstituted 1,2,3-triazole-sulfonamides 5a-n. This new methodology cleanly proceeded in w
Externí odkaz:
https://doaj.org/article/b27bac54f07e440d87f871000a39a53e
Autor:
Ayoub El Mahmoudi, Hamza Tachallait, Zakaria Moutaoukil, Suhana Arshad, Khalid Karrouchi, Rachid Benhida, Khalid Bougrin
Publikováno v:
ChemistrySelect. 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::774a107bfb3ed09adb944e54b7e2f452
https://doi.org/10.1002/slct.202203072
https://doi.org/10.1002/slct.202203072