يعرض 1 - 10 نتائج من 48 نتيجة بحث عن '"Mouhamad Jida"', وقت الاستعلام: 1.45s تنقيح النتائج
  1. 1
    دورية أكاديمية
    Pharmacomodulation of the Antimalarial Plasmodione: Synthesis of Biaryl- and N-Arylalkylamine Analogues, Antimalarial Activities and Physicochemical Properties

    المؤلفون: Karène Urgin, Mouhamad Jida, Katharina Ehrhardt, Tobias Müller, Michael Lanzer, Louis Maes, Mourad Elhabiri, Elisabeth Davioud-Charvet

    المصدر: Molecules, Vol 22, Iss 1, p 161 (2017)

    مصطلحات موضوعية: antimalarial, N-arylalkylamines, atovaquone, biaryls, menadione, 1,4-naphthoquinone, plasmodione, redox-cycling, reductive amination, Suzuki-Miyaura coupling, Organic chemistry, QD241-441

    وصف الملف: electronic resource

    Relation: http://www.mdpi.com/1420-3049/22/1/161; https://doaj.org/toc/1420-3049

    URL الوصول: https://doaj.org/article/53e798cd1fa64668a359e62aaa178e5c

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  2. 2
    3-Substituted 2-isocyanopyridines as versatile convertible isocyanides for peptidomimetic design

    المؤلفون: Steven Ballet, Evelien Renders, Bert U. W. Maes, Olivier Van der Poorten, Mathias Elsocht, Mouhamad Jida, Charlie Hollanders

    المساهمون: Chemistry, Faculty of Sciences and Bioengineering Sciences, Organic Chemistry

    المصدر: Chemical communications

    مصطلحات موضوعية: 2019-20 coronavirus outbreak, Coronavirus disease 2019 (COVID-19), Molecular Structure, Peptidomimetic, Chemistry, Pyridines, Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), Metals and Alloys, General Chemistry, Tripeptide, Combinatorial chemistry, Catalysis, Surfaces, Coatings and Films, Electronic, Optical and Magnetic Materials, chemistry.chemical_compound, Amide, Nitriles, Materials Chemistry, Ceramics and Composites, Molecule, Peptidomimetics

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::358539ce7eb0f0c3a7ea5b72ef8367c5
    https://pubmed.ncbi.nlm.nih.gov/34132258

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  3. 3
    Efficient One-Pot Access to Trisubstituted 2-Benzazepin-3-ones as Constrained Pseudopeptide Analogues and Privileged Scaffolds

    المؤلفون: Olivier Van der Poorten, Dirk Tourwé, Steven Ballet, Mouhamad Jida

    المصدر: Medicinal Chemistry. 14:400-408

    مصطلحات موضوعية: Molecular Structure, Peptidomimetic, Isocyanide, Imine, Molecular Conformation, Diastereomer, Stereoisomerism, Benzazepines, Combinatorial chemistry, chemistry.chemical_compound, Models, Chemical, chemistry, Reagent, Drug Discovery, Ugi reaction, Azepine, Bifunctional

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bfa1935b071284123fbeb5fcf6dbe5c3
    https://doi.org/10.2174/1573406413666171002122233

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  4. 4
    An Efficient One-Pot Synthesis of Chiral N-Protected 3-Substituted (Diketo)piperazines via Ugi-4CR/De-Boc/Cyclization Process

    المؤلفون: Steven Ballet, Mouhamad Jida

    المصدر: ChemistrySelect. 3:1027-1031

    مصطلحات موضوعية: 010405 organic chemistry, Chemistry, Scientific method, One-pot synthesis, General Chemistry, 010402 general chemistry, 01 natural sciences, Combinatorial chemistry, 0104 chemical sciences

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::0608855ee9cdc1fd4ea10c50d5a955e5
    https://doi.org/10.1002/slct.201702943

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  5. 5
    Efficient one-pot synthesis of enantiomerically pure N-protected-α-substituted piperazines from readily available α-amino acids

    المؤلفون: Steven Ballet, Mouhamad Jida

    المصدر: New Journal of Chemistry. 42:1595-1599

    مصطلحات موضوعية: chemistry.chemical_classification, 010405 organic chemistry, Chemistry, One-pot synthesis, General Chemistry, 010402 general chemistry, 01 natural sciences, Combinatorial chemistry, Catalysis, 0104 chemical sciences, Amino acid, Drug synthesis, Intramolecular force, Materials Chemistry, Protecting group

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::660c6e6f3473bdd316546707b2aa86c0
    https://doi.org/10.1039/c7nj04039c

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  6. 6
    A Platform of Regioselective Methodologies to Access Polysubstituted 2-Methyl-1,4-naphthoquinone Derivatives: Scope and Limitations

    المؤلفون: Jeremy Boilevin, David Lee Williams, Mouhamad Jida, Katharina Ehrhardt, Elisabeth Davioud-Charvet, Michael Lanzer, Elena Cesar Rodo, Liwen Feng, Don Antoine Lanfranchi, Max Bielitza

    المصدر: European Journal of Organic Chemistry. 2016:1982-1993

    مصطلحات موضوعية: 010405 organic chemistry, Organic Chemistry, 2 methyl 1 4 naphthoquinone, Regioselectivity, 010402 general chemistry, Ring (chemistry), 01 natural sciences, Cycloaddition, Naphthoquinone, 0104 chemical sciences, chemistry.chemical_compound, Menadione, chemistry, Propiophenone, Structural isomer, Organic chemistry, Physical and Theoretical Chemistry

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::59f7e15f3e13043a8ff8cf847a948218
    https://doi.org/10.1002/ejoc.201600144

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  7. 7
    3-Substituted isocyanopyridines as mildly convertible isocyanides

    المؤلفون: Karlijn Hollanders, Steven Bailet, Olivier Van der Poorten, Mouhamad Jida, Bert U. W. Maes, Mathias Elsocht

    المصدر: Proceedings of the 35th European Peptide Symposium.

    مصطلحات موضوعية: Chemistry, Convertible, Medicinal chemistry

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::87056c5bf712d5ee8539e062a636374a
    https://doi.org/10.17952/35eps.2018.118

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  8. 8
    Rapid construction of substituted 3-amino-1,5-benzothiazepin-4(5H)-one dipeptide scaffolds through an Ugi-4CR-Ullmann cross-coupling sequence

    المؤلفون: O. Van der Poorten, Karlijn Hollanders, Mouhamad Jida, Bert U. W. Maes, R. Van Den Hauwe, Dirk Tourwé, Steven Ballet

    المصدر: Organic and biomolecular chemistry

    مصطلحات موضوعية: Ullmann condensation, Dipeptide, 010405 organic chemistry, Chemistry, Stereochemistry, Organic Chemistry, Sequence (biology), 010402 general chemistry, 01 natural sciences, Biochemistry, 0104 chemical sciences, Coupling (electronics), chemistry.chemical_compound, Intramolecular force, Physical and Theoretical Chemistry, Conformational isomerism

    وصف الملف: pdf

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a40b7e4d9559d36fc7a57a41a1310d5f
    https://repository.uantwerpen.be/docman/irua/36e358/149126_2019_01_21.pdf

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  9. 9
    T3P-Promoted, Mild, One-Pot Syntheses of Constrained Polycyclic Lactam Dipeptide Analogues via Stereoselective Pictet–Spengler and Meyers Lactamization Reactions

    المؤلفون: Steven Ballet, Zofia Urbanczyk-Lipkowska, Olivier Van der Poorten, Dirk Tourwé, Karel Guillemyn, Mouhamad Jida

    المصدر: Organic Letters. 17:4482-4485

    مصطلحات موضوعية: Models, Molecular, Dipeptide, Lactams, Molecular Structure, Chemistry, Peptidomimetic, Phenylalanine, Organic Chemistry, Molecular Conformation, Organophosphonates, Stereoisomerism, Dipeptides, Biochemistry, Combinatorial chemistry, Anhydrides, chemistry.chemical_compound, Lactam, Organic chemistry, Stereoselectivity, Physical and Theoretical Chemistry

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d76bc2920169fc8d8c01179610836e23
    https://doi.org/10.1021/acs.orglett.5b02145

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  10. 10
    A Redox-Active Fluorescent pH Indicator for Detecting Plasmodium falciparum Strains with Reduced Responsiveness to Quinoline Antimalarial Drugs

    المؤلفون: Aurelia Geyer, Michael Lanzer, Cecilia P. Sanchez, Mouhamad Jida, Elisabeth Davioud-Charvet, Karène Urgin, Saravanan Mounien, Katharina Ehrhardt, Mourad Elhabiri

    المساهمون: Laboratoire de chimie moléculaire (LCM), Université de Strasbourg (UNISTRA)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Substances naturelles/chimie moléculaire, Université Louis Pasteur - Strasbourg I-Ecole européenne de chimie, polymères et matériaux [Strasbourg]-Centre National de la Recherche Scientifique (CNRS), Réponse immunitaire et developpement chez les insectes (RIDI - UPR 9002), Institut de biologie moléculaire et cellulaire (IBMC), Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Modèles Insectes de l'Immunité Innée (M3I), Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Laboratoire d'innovation moléculaire et applications (LIMA), Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA), Université de Strasbourg (UNISTRA)-Institut de biologie moléculaire et cellulaire (IBMC), Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)

    المصدر: ACS Infectious Diseases
    ACS Infectious Diseases, American Chemical Society, 2017, 3, pp.119-131. ⟨10.1021/acsinfecdis.5b00141⟩

    مصطلحات موضوعية: 0301 basic medicine, CBM, Mutant, Plasmodium falciparum, Drug Resistance, Protozoan Proteins, Drug resistance, Vacuole, Pharmacology, 03 medical and health sciences, Antimalarials, Chloroquine, parasitic diseases, medicine, Malaria, Falciparum, Fluorescent Dyes, 030102 biochemistry & molecular biology, biology, [CHIM.ORGA]Chemical Sciences/Organic chemistry, Membrane Transport Proteins, Transporter, Biological activity, Hydrogen-Ion Concentration, biology.organism_classification, 3. Good health, 030104 developmental biology, Infectious Diseases, Biochemistry, Drug development, Mutation, medicine.drug

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::811fb92cf68f303ddfbbcb0b19b270f5
    https://pubmed.ncbi.nlm.nih.gov/28183182

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