Home › Researcher directory › Ahmed Benharref A
Ahmed Benharref A
Affiliation : Cadi Ayyad University
- 232Publications (affiliation in Morocco)
- 486Total publications
- 3011Citations
- 29h-index
Research profile
Ahmed Benharref A has 232 indexed publications (2012–2026). Their work appears mainly in “Acta Crystallographica Section E Structure Reports Online”, “IUCrData” and “Journal of Molecular Structure”. Their most cited article, “Inhibitory effect of Atlas cedar essential oil on the corrosion of steel in 1 m HCl” (2018), has been cited 52 times. 13 of these publications date from the last three years of activity. Their work is co-authored with at least 12 researchers, including institutions in France, Spain, Canada.
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Create my free profile Add my publicationsResearch areas
- 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
Publication venues
- 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 per year
- 20261
- 20254
- 20248
- 20236
- 20223
- 20213
- 20208
- 20192
- 20187
- 201713
Collaborations
Partner institutions : Chouaib Doukkali University · University of Hassan II Casablanca · Centre National pour la Recherche Scientifique et Technique (CNRST) · Mohammed V University · Université Hassan II Mohammedia
Co-authors’ countries : France · Spain · Canada
Co-authors
- 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
Bibliographic data from OpenAlex (open database).
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