Accueil › Annuaire des chercheurs › Ahmed Benharref A
Ahmed Benharref A
Affiliation : Cadi Ayyad University
- 232Publications (affiliation marocaine)
- 486Publications au total
- 3011Citations
- 29Indice h
Profil de recherche
Ahmed Benharref A compte 232 publications référencées (2012–2026). Ses travaux paraissent principalement dans « Acta Crystallographica Section E Structure Reports Online », « IUCrData » et « Journal of Molecular Structure ». Son article le plus cité, « Inhibitory effect of Atlas cedar essential oil on the corrosion of steel in 1 m HCl » (2018), a été cité 52 fois. 13 de ces publications datent des trois dernières années d’activité. Ses travaux sont cosignés avec au moins 12 chercheurs, notamment dans des établissements de France, Espagne, Canada.
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Créer mon profil gratuit Ajouter mes publicationsDomaines de recherche
- Crystal structures of chemical compounds
- Crystallography and molecular interactions
- Crystal Structures and Properties
- Molecular spectroscopy and chirality
- Sesquiterpenes and Asteraceae Studies
Publications (232)
- Schiff Base-Sulfonamide Ligand and its Metal Complexes: Synthesis, Structural Characterization, Single-Crystal X-Ray Analysis, and Antioxidant Activity
- Stereoselective Synthesis and Characterization of Eudesmane Derivatives From α‐Costic Acid: DFT Approach and In Silico Evaluation Through Molecular Docking, MD Simulations, and ADMET Analysis
- Crystallographic and Computational Studies of Semisynthesized 4-Allyl-2-Methoxyphenyl-4-Nitrobenzenesulfonate
- Synthesis, Characterization, and Biological Evaluations of Eugenol–Amide Hybrids as Promising Antimicrobial Agents: Experimental and Computational Approaches
- Theoretical study of the molecular mechanism and regioselectivity of the (3+2) cycloaddition reaction between benzonitrile oxide and 2,4-dimethyl-2H-1,2,3-triazole and molecular docking studies of the obtained cycloadducts
- Mechanism and stereoselectivity of epoxidation reaction of a β-himachalene derivative: Insights from DFT, molecular docking, ADMET, and molecular dynamics investigations
- Ruthenium(II) Complex-Based Tetradentate Schiff Bases: Synthesis, Spectroscopic, Antioxidant, and Antibacterial Investigations
- Semisynthesis of new isoxazolines from (E)-α-atlantone: Antibacterial, antifungal activities, ADME-Tox, molecular docking, and molecular dynamics simulations investigations
- Quantum evaluation of novel epoxides: molecular docking, dynamics simulation, pharmacokinetics, stereoselectivity, and mechanistic insights into cis-himachalone and cis-himachalol epoxidation
- Synthesis, X-ray analysis, and antiviral evaluation of allohimachalol: Insights into stereoselectivity in epoxidation
- Comprehensive study on the stereoselective epoxidation of aromatic atlantone: mechanism, ADME analysis, and potential as COVID-19 drug
- Michael addition of ethyl acetoacetate on dibenzylideneacetone derivatives: Synthesis, spectroscopy, antimicrobial and in silico studies
- Semisynthesis and DFT Study of New Michael Adducts using (E)-α-Atlantone, Isolated from Cedrus atlantica Essential Oil
- Antiviral docking analysis, semisynthesis and mechanistic studies on the origin of stereo- and chemoselectivity in epoxidation reaction of α′-trans-Himachalene
- Oxidative functionalization of triterpenes isolated from Euphorbia resinifera latex: Semisynthesis, ADME-Tox, molecular docking, and molecular dynamics simulations
- MEDT Study, hemisynthesis via regioselective ring opening of α-Himachalene-Epoxides, ADME survey and docking studies designed to target coronavirus and HIV-1
- [2+1] Cycloaddition reaction of α-atlantone with m-CPBA in the light of experimental and MEDT quantum-chemical study
- Elucidating the selectivities and the mechanism of [3+2] cycloloaddition reaction between 9α-hydroxyparthenolide and 4-methylbenzene-nitrile-oxide
- Investigation of SARS-CoV-2 potential inhibition of some ingol derivatives, using Molecular Docking and dynamic simulation
- 3D-QSAR, ADME-Tox, and molecular docking of semisynthetic triterpene derivatives as antibacterial and insecticide agents
- Phytochemical Study: Molecular Docking of Eugenol Derivatives as Antioxidant and Antimicrobial Agents
- X-ray and DFT calculations of novel spiroisoxazolines derivatives
- Chemical reactivities and molecular docking studies of parthenolide with the main protease of HEP-G2 and SARS-CoV-2
- Divulging the regioselectivity of epoxides in the ring-opening reaction, and potential himachalene derivatives predicted to target the antibacterial activities and SARS-CoV-2 spike protein with docking study
- A Molecule of the Viridomycin Family Originating from a Streptomyces griseus-Related Strain Has the Ability to Solubilize Rock Phosphate and to Inhibit Microbial Growth
- Understanding the corrosion inhibition effectiveness using Senecio anteuphorbium L. fraction for steel in acidic media
- Optimization of Insecticidal Triterpene Derivatives by Biomimetic Oxidations with Hydrogen Peroxide and Iodosobenzene Catalyzed by MnIII and FeIII Porphyrin Complexes
- BF3·OEt2-Catalyzed Rearrangement of Epoxy-Himachalenes: Access to New Biosourced N-Acetamide-Based Himachalenes
- Versatile synthesis of cadalene and iso-cadalene from himachalene mixtures: Evidence and application of unprecedented rearrangements
- A regio- and stereoselectivity and molecular mechanism study on the addition reactions of morpholine and m-CPBA to 9α-hydroxyparthenolide using DFT calculations
- Rearrangement of Epoxide Derivatives Semisynthesized from β-Himachalene using Lewis and Bronsted Acids Catalysis
- Understanding the Mechanism and Selectivities of the Reaction of Meta-Chloroperbenzoic Acid and Dibromocarbene with β-Himachalene: A DFT Study
- Computational study of the mechanism and reactivity of -himachalene in presence of carbenes using DFT
- A theoretical study of regio and stereoselectivity nitration of thymol and carvacrol using DFT approach
- A DFT reinvestigation of chemo- and stereoselectivity epoxidation from α- and ɣ-trans himachalene with meta Chloroperoxybenzoic acid
- Inhibitory effect of Atlas cedar essential oil on the corrosion of steel in 1 m HCl
- The chemistry of the himachalenes and atlantones from Cedrus
- Semisynthetic Triterpenes Derived from Euphorbia officinarum as Plant Growth Promoters and Inducers of Disease Resistance
- Induced resistance to wild fire disease of Nicotiana benthamiana using seed treated with triterpene derivatives from Euphorbia
- Foliar application of the triterpene derivative 24-methylen-elemo-lanosta-8,24-dien-3-one alleviates salt toxicity in grapevine
- 1-(2-Isopropyl-4,7-dimethyl-3-nitronaphthalen-1-yl)ethanone
- 6-Methyl-1-(nitromethyl)-4-(propan-2-yl)naphthalene
- Antimicrobial Activity of two Semisynthetic Triterpene Derivatives from Euphorbia Officinarum Latex Against Fungal and Bacterial Phytopathogens
- Chemical Composition of Essential Oils and Mineral Contents ofZygophyllum gaetulum(Emb. and Maire)
- 2-Isopropyl-4,7-dimethyl-1-nitronaphthalene
- (1S,2R,8R)-11-Amino-2,2-dichloro-3,7,7,10-tetramethyltricyclo[6.4.0.01,3]dodec-10-en-9-one
- N-[1,4,4-Trimethyltricyclo[6.3.1.03,9]dodec-8(12)-en-2-yl]acetamide
- 1-(7-Isopropyl-2,5-dimethyl-8-nitronaphthalen-1-yl)ethanone
- N-[(3aR*,3bS*)-1,3b,7,7-Tetramethyl-3a,3b,4,5,6,7,7a,7b-octahydro-3H-cyclopenta[3,4]cyclobuta[1,2]benzen-3a-yl]acetamide
- N-[(1aR,5aR,8R,9aR)-1,1-Dichloro-1a,5,5,7-tetramethyl-1a,2,3,4,5,5a,8,9-octahydro-1H-benzo[a]cyclopropa[b][7]annulen-8-yl]acetamide
- A New Monoterpene Isolated from Nigella sativa Essential Oil
- 1-[(1R,2S,4R,7S)-3,3-Dichloro-4,11,11-trimethyltricyclo[5.4.0.02,4]undecan-7-yl]ethanone
- RELIABILITY OF SEMI-EMPIRICAL METHODS FOR THE DETERMINATION OF GEOMETRIC PARAMETERS OF ORGANIC COMPOUNDS β-HIMACHALENE HALGOGENATED
- (1S,3R,8R)-2,2-Dichloro-3,7,7,10-tetramethyl-11-methylenetricyclo[6.4.0.01,3]dodec-9-ene
- 6-Bromo-2-(1,4-dibromo-4-methylcyclohexyl)-6-methylheptan-4-one
- Triterpene derivatives from Euphorbia enhance resistance against Verticillium wilt of tomato
- Controlled Dimroth Rearrangement in the Suzuki–Miyaura Cross Coupling of Triazolopyridopyrimidines
- 1,6-Diacetyl-2-isopropyl-4,7-dimethylnaphthalene
- New Bioactive Semisynthetic Derivatives of 31-Norlanostenol and Obtusifoliol from Euphorbia Officinarum
- (1S,3R,8R,9S,10R)-2,2-Dichloro-3,7,7,10-tetramethyltricyclo[6.4.0.01,3]dodecan-9-yl 4-methylbenzene-1-sulfonate
- N′-[(1S,3R,8R)-2,2-Dichloro-3,7,7,10-tetramethyltricyclo[6.4.0.01,3]dodecan-11-yl]acetohydrazide
- Acid-promoted opening of 4,5- and 3,4-epoxy eudesmane scaffolds from α-isocostic acid
- Theoretical study of stereoselectivity of the [1 + 2] cycloaddition reaction between (1S,3R,8S)-2,2-dichloro-3,7,7,10-tetramethyltricyclo[6,4,0,01.3]dodec-9-ene and dibromocarbene using density functional theory (DFT) B3LYP/6-31G*(d)
- Selectivity controlled by ligand tuning in the palladium-catalysed cyclocarbonylation: Synthesis of new γ and δ lactones from a natural sesquiterpene
- Aromatization of (Z) and (E)-α-atlantones isolated from Cedrus atlantica essential oil followed by condensation with thiosemicarbazide: synthesis of new thiadiazolines derivatives
- Crystal structure of 1-isopropyl-4,7-dimethyl-3-nitronaphthalene
- Crystal structure of (1S,3R,8R,9S,10R)-10-bromomethyl-2,2-dichloro-9,10-epoxy-3,7,7-trimethyltricyclo[6.4.0.01,3]dodecane
- Crystal structure of (1S,2R,4R,9S,11S,12R)-9α-hydroxy-4,8-dimethyl-12-[(thiomorpholin-4-yl)methyl]-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-13-one
- Crystal structure of (1S,3R,8R,9R,10S)-2,4,6-tris(2,2-dichloro-3,7,7,10-tetramethyltricyclo[6.4.0.01,3]dodec-9-yl)cyclotriboroxane
- Synthesis and biological evaluation of 9α- and 9β-hydroxyamino-parthenolides as novel anticancer agents
- Solvent-free epoxidation of himachalenes and their derivatives by TBHP using [MoO2(SAP)]2 as a catalyst
- 1-[(1S,6R,7S,9R)-8,8-Dibromo-5,5,9-trimethyltricyclo[4.4.0.17,9]decan-1-yl]ethanone
- (1R,4R,6S,7R)-5,5-Dibromo-1,4,8,8-tetramethyltricyclo[5.4.1.04,6]dodecan-12-one
- Understanding the Regioselectivity and Reactivity of β-Himachalene Using Zeroual Function as a new Regioselectivity Descriptor
- 12-{[4-(4-Bromophenyl)piperazin-1-yl]methyl}-9α-hydroxy-4,8-dimethyl-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-13-one
- Theoretical study of regioselectivity and stereoselectivity of condensation of β-himachalene with dichlorocarbene using density functional theory (DFT)
- Experimental and theoretical studie of the chemicals shifts (13C NMR) of some cyclic products by the method DFT
- (1S,2R,3S,6S,7R)-3,7,11,11-Tetramethyl-6,7-epoxybicyclo[5.4.0]undecane-2-ol
- Theoretical study of the chemo-, regio- and stereoselectivity of the interaction between dichlorocarbene and α-trans-himachalene using density functional theory (DFT) B3LYP/6-31G (d, p)
- 9α-Hydroxy-12-{[4-(4-hydroxyphenyl)piperazin-1-yl]methyl}-4,8-dimethyl-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-13-one
- (1S,3R,8R,9R,10S)-2,2-Dibromo-3,7,7,10-tetramethyl-9β,10β-epoxy-3,7,7,10-tetramethyltricyclo[6.4.0.01,3]dodecane
- (1S,3S,8R,9S,11R)-10,10-Dichloro-3,7,7,11-tetramethyltetracyclo[6.5.0.01,3.09,11]tridecane
- (1S,3R,8R,9S,11R)-2,2,10,10-Tetrachloro-3,7,7,11-tetramethyltetracyclo[6.5.0.01,3.09,11]tridecane
- 2,2-Dichloro-3,7,7,11-tetramethyl-10-azatetracyclo[6.5.0.01,3.09,11]tridecane
- (1S,2R,7R,8S,10R)-9,9-Dibromo-2,6,6,10-tetramethyl-1α,2α-epoxytricyclo[5.5.0.08,10]dodecane
- (1S,3R,8R)-2,2-Dichloro-3,7,7,10-tetramethyltricyclo[6.4.0.01,3]dodec-9-en-11-one
- (1S,3R,8R,9S,11R)-2,2-Dibromo-10,10-dichloro-3,7,7,11-tetramethyltetracyclo[6.5.0.01,3.09,11]tridecane
- (1S,3R,8R,9S,11R)-10,10-Dibromo-2,2-dichloro-3,7,7,11-tetramethyltetracyclo[6.5.0.01,3.09,11]tridecane
- (1S,3R,8R,10R)-2,2-Dibromo-3,7,7,10-tetramethyltricyclo[6.4.0.01,3]dodecan-9-one
- (1S,3R,8R,11S)-11-Bromo-10-bromomethyl-2,2-dichloro-3,7,7-trimethyltricyclo[6.4.0.01,3]dodec-9-ene
- (1S,3S,8R,9S,11R)-10,10-Dibromo-3,7,7,11-tetramethyltetracyclo[6.5.0.01,3.09,11]tridecane
- (1R,4R,6S,7S)-5,5-Dichloro-1,4,8,8-tetramethyltricyclo[5.4.11,7.04,6]dodecan-12-one
- (1S,3S,8R,10R,11R)-3,7,7,10-Tetramethyltricyclo[6.4.0.01,3]dodecan-11-ol
- 1,10,10-Trimethyl-5-phenyl-3-oxa-4-azatricyclo[5.2.1.02,6]dec-4-en-2-ol
- Prenatal exposure to tobacco extract containing nicotinic alkaloids produces morphological and behavioral changes in newborn rats
- Access to new sequiterpenoids by catalytic acid rearrangement of 9α-hydroxyparthenolide
- (1S,3R,8R)-2,2-Dibromo-3,7,7,10-tetramethyltricyclo[6.4.0.01,3]dodec-9-ene
- 10α-Hydroxy-13-{[4-(2-hydroxyphenyl)piperazin-1-yl]methyl}-4,9-dimethyl-3,8,15-trioxatetracyclo[10.3.0.02,4.07,9]pentadecan-14-one
- Methyl 2-(4a,8-Dimethyl-7-oxodecahydronaphthalen-2-yl)acrylate
- 9β-Hydroxy-6,9-dimethyl-3-methylene-3a,4,8,9,9a,9b-hexahydroazuleno[4,5-b]furan-2(3H)-one
Revues de publication
- Acta Crystallographica Section E Structure Reports Online × 23
- IUCrData × 14
- Journal of Molecular Structure × 8
- International journal of innovation and applied studies × 5
- Chemistry of Heterocyclic Compounds × 4
- Acta Crystallographica Section E Crystallographic Communications × 4
Publications par année
- 20261
- 20254
- 20248
- 20236
- 20223
- 20213
- 20208
- 20192
- 20187
- 201713
Collaborations
Établissements partenaires : Chouaib Doukkali University · University of Hassan II Casablanca · Centre National pour la Recherche Scientifique et Technique (CNRST) · Mohammed V University · Université Hassan II Mohammedia
Pays des co-auteurs : France · Espagne · Canada
Co-auteurs
- Moha Berraho
- Noureddine Mazoir
- Lahcen El Ammari
- Mohamed Saadi
- Mohamed Akssira A
- Mohamed Moumou
- Abdelouahd Oukhrib
- Aziz Auhmani
- Abdellah Zeroual
- Essêdiya Lassaba
- Mohamed Dakir
- Ahmed El Hakmaoui
Données bibliographiques issues d’OpenAlex (base ouverte).
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