5 results on '"Abdellah N'ait Ousidi"'
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2. Design, Synthesis, Cytotoxic Effect Evaluation and Molecular Docking of (R)‐Camphor‐Based Thiazolidinone‐Isoxazole and Thiazolidinone‐1,2,3‐triazole Hybrids'
- Author
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Abdellah N'ait Ousidi, Abdoullah Bimoussa, Mohammed Loubidi, Mourad Fawzi, Yassine Laamari, Ali Oubella, Mohamed Maatallah, Sabine Berteina‐Raboin, Aziz Auhmani, Mohamed Labd Taha, Hamid Morjani, and Moulay Youssef Ait Itto
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General Chemistry - Published
- 2023
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3. Electrochemical and theoretical studies of some monoterpenic thiazolidinones as corrosion inhibitors for steel in acidic media
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Aziz Auhmani, Abdellah N'ait Ousidi, Rachid Idouhli, Mohy Eddine Khadiri, My Youssef Ait Itto, A. Abouelfida, and Abdelaziz Benyaich
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Materials science ,Hydrochloric acid ,030206 dentistry ,02 engineering and technology ,Surfaces and Interfaces ,General Chemistry ,021001 nanoscience & nanotechnology ,Electrochemistry ,Surfaces, Coatings and Films ,Corrosion ,03 medical and health sciences ,chemistry.chemical_compound ,0302 clinical medicine ,Adsorption ,chemistry ,Mechanics of Materials ,Materials Chemistry ,0210 nano-technology ,Nuclear chemistry - Abstract
This work deals with the study of the inhibition activity of three thiazolidinones (prepared from monoterpenic ketones) on the deterioration of S300 steel in hydrochloric acid solution. The potenti...
- Published
- 2020
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4. Crystal structure of dimethyl 2-((2 Z ,5 Z )-5-(2-methoxy-2-oxoethylidene)-2-{( E )-[2-methyl-5-(prop-1-en-2-yl)cyclohex-2-enylidene]hydrazinylidene}-4-oxothiazolidin-3-yl)fumarate
- Author
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Abdelwahed Auhmani, Aziz Auhmani, Abdellah N'ait Ousidi, Jean-Claude Daran, Abdelkhalek Riahi, My Youssef Ait Itto, Laboratoire de Physico-Chimie Moléculaire et Synthèse Organique, Département de Chimie, Faculté des Sciences, Faculté des Sciences Semlalia Marrakech, Institut de Chimie Moléculaire de Reims - UMR 7312 (ICMR), SFR Condorcet, Université de Reims Champagne-Ardenne (URCA)-Université de Picardie Jules Verne (UPJV)-Centre National de la Recherche Scientifique (CNRS)-Université de Reims Champagne-Ardenne (URCA)-Université de Picardie Jules Verne (UPJV)-Centre National de la Recherche Scientifique (CNRS)-SFR CAP Santé (Champagne-Ardenne Picardie Santé), Université de Reims Champagne-Ardenne (URCA)-Université de Picardie Jules Verne (UPJV)-Université de Reims Champagne-Ardenne (URCA)-Université de Picardie Jules Verne (UPJV)-Université de Reims Champagne-Ardenne (URCA)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Laboratoire de chimie de coordination (LCC), Institut National Polytechnique (Toulouse) (Toulouse INP), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Institut de Chimie de Toulouse (ICT-FR 2599), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), and Université Fédérale Toulouse Midi-Pyrénées-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)
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Stereochemistry ,Hydrazone ,Crystal structure ,010403 inorganic & nuclear chemistry ,Ring (chemistry) ,01 natural sciences ,Natural product ,Research Communications ,lcsh:Chemistry ,chemistry.chemical_compound ,General Materials Science ,[CHIM.COOR]Chemical Sciences/Coordination chemistry ,chemistry.chemical_classification ,010405 organic chemistry ,General Chemistry ,Meth ,Condensed Matter Physics ,3. Good health ,0104 chemical sciences ,Thiazolidine derivatives ,chemistry ,lcsh:QD1-999 ,thiazolidine derivatives ,Heterocyclic compounds ,Derivative (chemistry) - Abstract
The crystal structure of the title compound, dimethyl 2-((2Z,5Z)-5-(2-methoxy-2-oxoethylidene)-2-{(E)-[2-methyl-5-(prop-1-en-2-yl)cyclohex-2-enylidene]hydrazinylidene}-4-oxothiazolidin-3-yl)fumarate displays a conformational disorder which inverts the configuration of the chiral C atom within the cyclohexylidene ring., The crystal structure and the conformation of the title compound, C22H27N3O7S, were determined from the synthetic pathway and by X-ray analysis. This compound is a new 4-thiazolidinone derivative prepared and isolated as pure product from thiosemicarbazone carvone. The molecule is built up from an oxothiazolidine ring tetrasubstituted by a methoxy–oxoethylidene, a maleate, an oxygen and a cyclohexylidene–hydrazone. The cyclohexylidene ring is statistically disordered over two positions, resulting in an inversion of configuration for the substituted carbon.
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- 2017
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5. Crystal structure of 2-[(3aS,6R)-3,3,6-trimethyl-3,3a,4,5,6,7-hexahydro-2H-indazol-2-yl]thiazol-4(5H)-one
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Jean-Claude Daran, Abdellah N'ait Ousidi, Auhmani Abdelwahed, Aziz Auhmani, Abdelkhalek Riahi, My Youssef Ait Itto, Laboratoire de Physico-Chimie Moléculaire et Synthèse Organique, Département de Chimie, Faculté des Sciences, Faculté des Sciences Semlalia Marrakech, Institut de Chimie Moléculaire de Reims - UMR 7312 (ICMR), SFR Condorcet, Université de Reims Champagne-Ardenne (URCA)-Université de Picardie Jules Verne (UPJV)-Centre National de la Recherche Scientifique (CNRS)-Université de Reims Champagne-Ardenne (URCA)-Université de Picardie Jules Verne (UPJV)-Centre National de la Recherche Scientifique (CNRS)-SFR CAP Santé (Champagne-Ardenne Picardie Santé), Université de Reims Champagne-Ardenne (URCA)-Université de Picardie Jules Verne (UPJV)-Université de Reims Champagne-Ardenne (URCA)-Université de Picardie Jules Verne (UPJV)-Université de Reims Champagne-Ardenne (URCA)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Laboratoire de chimie de coordination (LCC), Institut National Polytechnique (Toulouse) (Toulouse INP), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Institut de Chimie de Toulouse (ICT-FR 2599), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), and Université Fédérale Toulouse Midi-Pyrénées-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)
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crystal structure ,Stereochemistry ,C—H⋯O hydrogen bonding ,Crystal structure ,Pyrazole ,010402 general chemistry ,Ring (chemistry) ,C—H⋯π interactions ,01 natural sciences ,thiazolidinone ,Research Communications ,Crystal ,chemistry.chemical_compound ,C—H...π interactions ,heterocyclic compounds ,General Materials Science ,[CHIM.COOR]Chemical Sciences/Coordination chemistry ,C—H...O hydrogen bonding ,Indazole ,Crystallography ,010405 organic chemistry ,Hydrogen bond ,General Chemistry ,Condensed Matter Physics ,HEXA ,thiazolidinone ,3. Good health ,0104 chemical sciences ,chemistry ,QD901-999 ,indazole ,absolute structure ,Derivative (chemistry) - Abstract
The absolute structure of the title compound was determined from the synthetic pathway and by resonant scattering. The compound is a new thiazolidin-4-one derivative, prepared from (R)-thiosemicarbazone pulegone, and was isolated on crystallization from ethanol as the pure (3aS,6R)-diastereisomer., The title compound, C13H19N3OS, is a new thiazolidin-4-one derivative prepared and isolated as the pure (3aS,6R)-diastereisomer from (R)-thiosemicarbazone pulegone. It crystallized with two independent molecules (A and B) in the asymmetric unit. The compound is composed of a hexhydroindazole ring system (viz. a five-membered dihydropyrazole ring fused to a cyclohexyl ring) with a thiazole-4-one ring system attached to one of the pyrazole N atoms (at position 2). The overall geometry of the two molecules differs slightly, with the mean planes of the pyrazole and thiazole rings being inclined to one another by 10.4 (1)° in molecule A and 0.9 (1)° in molecule B. In the crystal, the A and B molecules are linked via C—H⋯O hydrogen bonds, forming slabs parallel to the ab plane. There are C—H⋯π interactions present within the layers, and between the layers, so forming a three-dimensional structure.
- Published
- 2016
- Full Text
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