يعرض 1 - 10 نتائج من 50 نتيجة بحث عن '"Muriel Amatore"', وقت الاستعلام: 0.88s تنقيح النتائج
  1. 1
    N ‐Heterocyclic Carbene Control over Multiple Stereogenicities: Atroposelective Synthesis of Axially Chiral Phthalimides

    المؤلفون: Manuel Barday, Jessica Rodrigues, Pierre Bouillac, Jean Rodriguez, Muriel Amatore, Thierry Constantieux

    المصدر: Advanced Synthesis & Catalysis. 365:148-155

    مصطلحات موضوعية: General Chemistry

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::99cd2e31c0f4e4fe6a45463a14d7c884
    https://doi.org/10.1002/adsc.202201175

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  2. 2
    Enolate Surrogates and Unusual Nucleophiles in Stereoselective Iridium-catalyzed Allylic Substitutions

    المؤلفون: Pierre Bouillac, Manuel Barday, Thierry Constantieux, Muriel Amatore

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::d0eb03302f1df34fda79e5a4a620ba41
    https://doi.org/10.1142/9789811248436_0011

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  3. 3
    Synthesis and Electron Accepting Properties of Two Di(benz[

    المؤلفون: Bruno, Salgues, Rudraditya, Sarkar, Muhammad Luthfi, Fajri, Yatzil Alejandra, Avalos-Quiroz, Anne-Doriane, Manick, Michel, Giorgi, Nicolas, Vanthuyne, Yannick, Carissan, Christine, Videlot-Ackermann, Jörg, Ackermann, Gabriel, Canard, Jean-Luc, Parrain, Boris, Le Guennic, Denis, Jacquemin, Muriel, Amatore, Laurent, Commeiras, Elena, Zaborova, Frédéric, Fages

    المصدر: The Journal of organic chemistry. 87(5)

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::310dbc78b6c1b2d986ee56cb7c6207e1
    https://pubmed.ncbi.nlm.nih.gov/35176857

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  4. 4
    Alkyne Surrogates in Cycloaddition Reactions for the Preparation of Molecules of Interest

    المؤلفون: Muriel Amatore, Laurent Commeiras, Jean-Luc Parrain

    المساهمون: Institut des Sciences Moléculaires de Marseille (ISM2), Aix Marseille Université (AMU)-École Centrale de Marseille (ECM)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)

    المصدر: Asian Journal of Organic Chemistry
    Asian Journal of Organic Chemistry, Wiley, 2021, 10 (9), pp.2287-2299. ⟨10.1002/ajoc.202100345⟩
    Asian Journal of Organic Chemistry, 2021, 10 (9), pp.2287-2299. ⟨10.1002/ajoc.202100345⟩

    مصطلحات موضوعية: chemistry.chemical_classification, heterocycles, 010405 organic chemistry, [CHIM.ORGA]Chemical Sciences/Organic chemistry, Organic Chemistry, carbocycles, Alkyne, 010402 general chemistry, 01 natural sciences, Combinatorial chemistry, Cycloaddition, 0104 chemical sciences, chemistry, alkyne equivalent, Molecule, alkyne surrogate, cycloaddition

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed5966f12e38d839a47ab7529e979444
    https://hal.archives-ouvertes.fr/hal-03423100

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  5. 5
    Enantioselective Organocatalytic Syntheses and Ring‐Expansions of Cyclobutane Derivatives

    المؤلفون: Pierre Bouillac, Yoann Coquerel, Manuel Barday, Muriel Amatore, Jean Rodriguez, Thierry Constantieux

    المساهمون: Institut des Sciences Moléculaires de Marseille (ISM2), Aix Marseille Université (AMU)-École Centrale de Marseille (ECM)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)

    المصدر: European Journal of Organic Chemistry
    European Journal of Organic Chemistry, Wiley-VCH Verlag, 2021, 2021 (21), pp.3023-3034. ⟨10.1002/ejoc.202100405⟩
    European Journal of Organic Chemistry, 2021, 2021 (21), pp.3023-3034. ⟨10.1002/ejoc.202100405⟩

    مصطلحات موضوعية: Annulation, 010405 organic chemistry, Chemistry, Organocatalysis, [CHIM.ORGA]Chemical Sciences/Organic chemistry, Organic Chemistry, Enantioselective synthesis, Medium-ring compounds, Ring expansion, Strained molecules, [CHIM.CATA]Chemical Sciences/Catalysis, 010402 general chemistry, Ring (chemistry), Small ring systems, 01 natural sciences, Chemical synthesis, Combinatorial chemistry, 0104 chemical sciences, Cyclobutane, chemistry.chemical_compound, Molecule, Stereoselectivity, Physical and Theoretical Chemistry

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10515a26c033efc25c6530160ed6c29f
    https://hal.archives-ouvertes.fr/hal-03370300

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  6. 6
    Access to Fluorenones Using Benzocyclopentynone Surrogate as Partner for the [2 + 2 + 2] Cycloaddition Reaction

    المؤلفون: Frédéric Fages, Muriel Amatore, Jean-Luc Parrain, Elena Zaborova, Anne-Doriane Manick, Bruno Salgues, Laurent Commeiras

    المساهمون: Institut des Sciences Moléculaires de Marseille (ISM2), Aix Marseille Université (AMU)-École Centrale de Marseille (ECM)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Centre Interdisciplinaire de Nanoscience de Marseille (CINaM), Centre National de la Recherche Scientifique (CNRS)-Aix Marseille Université (AMU), Aix Marseille Université (AMU)-Centre National de la Recherche Scientifique (CNRS)

    المصدر: Organic Letters
    Organic Letters, American Chemical Society, 2020, 22 (5), pp.1894-1898. ⟨10.1021/acs.orglett.0c00235⟩
    Organic Letters, 2020, 22 (5), pp.1894-1898. ⟨10.1021/acs.orglett.0c00235⟩

    مصطلحات موضوعية: 010405 organic chemistry, [CHIM.ORGA]Chemical Sciences/Organic chemistry, Organic Chemistry, chemistry.chemical_element, 010402 general chemistry, 01 natural sciences, Biochemistry, Combinatorial chemistry, Cycloaddition, 0104 chemical sciences, Catalysis, Rhodium, chemistry.chemical_compound, fluorenone, chemistry, Fluorenone, Molecule, Physical and Theoretical Chemistry, alkyne surrogate

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8eb2204f5e34a01dd09a61a1c63ffaea
    https://hal.archives-ouvertes.fr/hal-02873529

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  7. 7
    When cobalt-mediated [2 + 2 + 2] cycloaddition reaction dares go astray: synthesis of unprecedented cobalt( iii )-complexes

    المؤلفون: Corinne Aubert, Marion Delorme, Paola Nava, Alexander Punter, Muriel Amatore, Laurent Commeiras, Raquel Oliveira, Yannick Carissan, Jean-Luc Parrain

    المساهمون: Institut des Sciences Moléculaires de Marseille (ISM2), Aix Marseille Université (AMU)-École Centrale de Marseille (ECM)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Processus d'Activation Sélective par Transfert d'Energie Uni-électronique ou Radiatif (UMR 8640) (PASTEUR), Département de Chimie - ENS Paris, École normale supérieure - Paris (ENS Paris), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-École normale supérieure - Paris (ENS Paris), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Institut Parisien de Chimie Moléculaire (IPCM), Chimie Moléculaire de Paris Centre (FR 2769), Institut de Chimie du CNRS (INC)-École normale supérieure - Paris (ENS Paris), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Centre National de la Recherche Scientifique (CNRS)-Ecole Nationale Supérieure de Chimie de Paris - Chimie ParisTech-PSL (ENSCP), Université Paris sciences et lettres (PSL)-Ecole Superieure de Physique et de Chimie Industrielles de la Ville de Paris (ESPCI Paris), Université Paris sciences et lettres (PSL)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut de Chimie du CNRS (INC)-École normale supérieure - Paris (ENS Paris), Université Paris sciences et lettres (PSL)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), École normale supérieure - Paris (ENS-PSL), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-École normale supérieure - Paris (ENS-PSL), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Ecole Nationale Supérieure de Chimie de Paris - Chimie ParisTech-PSL (ENSCP), Université Paris sciences et lettres (PSL)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-École normale supérieure - Paris (ENS-PSL), Université Paris sciences et lettres (PSL)-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS)

    المصدر: Dalton Transactions
    Dalton Transactions, Royal Society of Chemistry, 2019, 48 (42), pp.15767-15771. ⟨10.1039/C9DT03311D⟩
    Dalton Transactions, 2019, 48 (42), pp.15767-15771. ⟨10.1039/C9DT03311D⟩

    مصطلحات موضوعية: 010405 organic chemistry, [CHIM.ORGA]Chemical Sciences/Organic chemistry, chemistry.chemical_element, Mots Clefs Cycloaddition, Cobalt, 010402 general chemistry, 01 natural sciences, Medicinal chemistry, butenolide, Cycloaddition, 0104 chemical sciences, Inorganic Chemistry, Fragmentation (mass spectrometry), chemistry, Moiety, Ene reaction, complex, Butenolide

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0dafbc81240fdc41dc46433be9e0c8ef
    https://hal.archives-ouvertes.fr/hal-02354762/document

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  8. 8
    Hydroboration and Diboration of Internal Alkynes Catalyzed by a Well-Defined Low-Valent Cobalt Catalyst

    المؤلفون: Ye Lyu, Muriel Amatore, Laura Ferrand, Marc Petit, Alejandro Rivera-Hernández, Corinne Aubert, Brendan J. Fallon

    المساهمون: Institut Parisien de Chimie Moléculaire (IPCM), Institut de Chimie du CNRS (INC)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Centre National de la Recherche Scientifique (CNRS), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)

    المصدر: Synthesis
    Synthesis, 2017, 49 (17), pp.3895--3904. ⟨10.1055/s-0036-1588996⟩
    Synthesis: Journal of Synthetic Organic Chemistry
    Synthesis: Journal of Synthetic Organic Chemistry, 2017, 49 (17), pp.3895--3904. ⟨10.1055/s-0036-1588996⟩

    مصطلحات موضوعية: Reaction conditions, 010405 organic chemistry, Organic Chemistry, Regioselectivity, chemistry.chemical_element, 010402 general chemistry, 01 natural sciences, Medicinal chemistry, Catalysis, 0104 chemical sciences, Cobalt catalyst, Hydroboration, chemistry, Organic chemistry, [CHIM]Chemical Sciences, Stereoselectivity, Cobalt, ComputingMilieux_MISCELLANEOUS

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10686b354e7436ef29943cc4dcb50a2d
    https://hal.archives-ouvertes.fr/hal-01644384

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  9. 9
    Recent Advances in Stereoselective [2+2+2] Cycloadditions

    المؤلفون: Corinne Aubert, Muriel Amatore

    المصدر: European Journal of Organic Chemistry. 2015:265-286

    مصطلحات موضوعية: 010405 organic chemistry, Stereochemistry, Chemistry, Organic Chemistry, Chiral ligand, Enantioselective synthesis, 010402 general chemistry, 01 natural sciences, Combinatorial chemistry, Cycloaddition, 0104 chemical sciences, Catalysis, Intramolecular force, Molecule, Stereoselectivity, Physical and Theoretical Chemistry, Chirality (chemistry)

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::455ce9b020f523e4fd55fb1dcd55548d
    https://doi.org/10.1002/ejoc.201403012

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  10. 10
    Regio- and Stereoselective Hydrosilylation of Unsymmetrical Alkynes Catalyzed by a Well-Defined, Low-Valent Cobalt Catalyst

    المؤلفون: Cédric Simon, Geoffrey Gontard, Muriel Amatore, Etienne Derat, Marc Petit, Alejandro Rivera-Hernández, Sandrine Ventre, Marie-Hélène Tremblay, Corinne Aubert, Brendan J. Fallon

    المساهمون: Institut Parisien de Chimie Moléculaire (IPCM), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), CNRS, MRES, UPMC, CONACYT [252113], ANR-12-BS07-0031,CoCaCoLight,Activation de liaisons par des complexes de Cobalt(I) et fonctionnalisation assistée par la lumière(2012)

    المصدر: Organic Letters
    Organic Letters, 2016, 18 (17), pp.4242-4245. ⟨10.1021/acs.orglett.6b01987⟩
    Organic Letters, American Chemical Society, 2016, 18 (17), pp.4242-4245. ⟨10.1021/acs.orglett.6b01987⟩

    مصطلحات موضوعية: 010405 organic chemistry, Hydrosilylation, [CHIM.ORGA]Chemical Sciences/Organic chemistry, Organic Chemistry, chemistry.chemical_element, 010402 general chemistry, 01 natural sciences, Biochemistry, Combinatorial chemistry, 0104 chemical sciences, Catalysis, Cobalt catalyst, chemistry.chemical_compound, chemistry, Organic chemistry, Stereoselectivity, Physical and Theoretical Chemistry, Cobalt

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63efcd214bf60852cd64acc101c7bb54
    https://hal.science/hal-01397954

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