يعرض 1 - 10 نتائج من 12 نتيجة بحث عن '"Aymen Skhiri"', وقت الاستعلام: 0.83s تنقيح النتائج
  1. 1
    دورية أكاديمية
    Reactivity of bromoselenophenes in palladium-catalyzed direct arylations

    المؤلفون: Aymen Skhiri, Ridha Ben Salem, Jean-François Soulé, Henri Doucet

    المصدر: Beilstein Journal of Organic Chemistry, Vol 13, Iss 1, Pp 2862-2868 (2017)

    مصطلحات موضوعية: C–H bond activation, catalysis, heteroarenes, palladium, selenophene, Science, Organic chemistry, QD241-441

    وصف الملف: electronic resource

    Relation: https://doaj.org/toc/1860-5397

    URL الوصول: https://doaj.org/article/47b51a78d0b5414bb4953bbcb062c412

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  2. 2
    Experimental and theoretical studies of the rhodium(i)-catalysed C–H oxidative alkenylation/cyclization of N-(2-(methylthio)phenyl)benzamides with maleimides

    المؤلفون: Aymen Skhiri, Attila Taborosi, Nozomi Ohara, Yusuke Ano, Seiji Mori, Naoto Chatani

    المصدر: Organic Chemistry Frontiers. 10:1617-1625

    مصطلحات موضوعية: Organic Chemistry

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::c52e463cc574c29b2c0d465e445ecc12
    https://doi.org/10.1039/d3qo00023k

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  3. 3
    Effects of Silver Carbonate and p-Nitrobenzoic Acid for Accelerating Palladium-Catalyzed Allylic C–H Acyloxylation

    المؤلفون: Hayato Tsurugi, Kazushi Mashima, Masahiko Seki, Aymen Skhiri, Haruki Nagae

    المصدر: Organic Letters. 23:7044-7048

    مصطلحات موضوعية: inorganic chemicals, Allylic rearrangement, Organic Chemistry, Substrate (chemistry), chemistry.chemical_element, Biochemistry, Medicinal chemistry, Catalysis, chemistry.chemical_compound, chemistry, P-nitrobenzoic acid, Carboxylate, Physical and Theoretical Chemistry, Selectivity, Silver carbonate, Palladium

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::85cd479c0b5381c3c1b86db43c5c3bb0
    https://doi.org/10.1021/acs.orglett.1c02406

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  4. 4
    Effects of Silver Carbonate and

    المؤلفون: Aymen, Skhiri, Haruki, Nagae, Hayato, Tsurugi, Masahiko, Seki, Kazushi, Mashima

    المصدر: Organic letters. 23(18)

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::f651f565fd1ec3d21a602f1c3e9830a0
    https://pubmed.ncbi.nlm.nih.gov/34752119

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  5. 5
    Nickel-Catalyzed Reaction of Benzamides with Bicylic Alkenes: Cleavage of C–H and C–N Bonds

    المؤلفون: Naoto Chatani, Aymen Skhiri

    المصدر: Organic Letters. 21:1774-1778

    مصطلحات موضوعية: Bicyclic molecule, 010405 organic chemistry, Chemistry, Organic Chemistry, chemistry.chemical_element, 010402 general chemistry, Cleavage (embryo), 01 natural sciences, Biochemistry, Medicinal chemistry, 0104 chemical sciences, Catalysis, Nickel, chemistry.chemical_compound, Group (periodic table), Physical and Theoretical Chemistry, Norbornene

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be76114e211641768c06ad5796d404ce
    https://doi.org/10.1021/acs.orglett.9b00351

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  6. 6
    Correction to 'Effects of Silver Carbonate and p-Nitrobenzoic Acid for Accelerating Palladium-Catalyzed Allylic C–H Acyloxylation'

    المؤلفون: Masahiko Seki, Kazushi Mashima, Aymen Skhiri, Haruki Nagae, Hayato Tsurugi

    المصدر: Organic Letters. 23:9012-9012

    مصطلحات موضوعية: Allylic rearrangement, chemistry.chemical_compound, chemistry, Organic Chemistry, P-nitrobenzoic acid, chemistry.chemical_element, Physical and Theoretical Chemistry, Biochemistry, Medicinal chemistry, Silver carbonate, Catalysis, Palladium

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::9b8359bf9a654a396008706f7367b3a9
    https://doi.org/10.1021/acs.orglett.1c03676

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  7. 7
    Pd-Catalysed Direct Arylation of Heteroaromatics Using (Poly)halobenzenesulfonyl Chlorides as Coupling Partners: One Step Access to (Poly)halo-Substituted Bi(hetero)aryls

    المؤلفون: Henri Doucet, Kedong Yuan, Anissa Beladhria, Jean-François Soulé, Aymen Skhiri, Ridha Ben Salem

    المصدر: European Journal of Organic Chemistry. 2015:4428-4436

    مصطلحات موضوعية: 010405 organic chemistry, Organic Chemistry, Substituent, chemistry.chemical_element, Regioselectivity, Homogeneous catalysis, 010402 general chemistry, Cleavage (embryo), Ring (chemistry), 01 natural sciences, Medicinal chemistry, 0104 chemical sciences, chemistry.chemical_compound, chemistry, Organic chemistry, Reactivity (chemistry), Physical and Theoretical Chemistry, Benzene, Palladium

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::5ddaac81260e7c200dd04dc6dfe63bd7
    https://doi.org/10.1002/ejoc.201500354

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  8. 8
    Reactivity of bromoselenophenes in palladium-catalyzed direct arylations

    المؤلفون: Ridha Ben Salem, Henri Doucet, Jean-François Soulé, Aymen Skhiri

    المساهمون: Institut des Sciences Chimiques de Rennes (ISCR), Université de Rennes 1 (UR1), Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-Institut National des Sciences Appliquées - Rennes (INSA Rennes), Institut National des Sciences Appliquées (INSA)-Université de Rennes (UNIV-RENNES)-Institut National des Sciences Appliquées (INSA)-Ecole Nationale Supérieure de Chimie de Rennes (ENSCR)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Université de Sfax - University of Sfax, CNRS, Scientific Ministry of Higher Education and Research of Tunisia, Rennes Metropole, Université de Rennes (UR)-Institut National des Sciences Appliquées - Rennes (INSA Rennes), Institut National des Sciences Appliquées (INSA)-Institut National des Sciences Appliquées (INSA)-Ecole Nationale Supérieure de Chimie de Rennes (ENSCR)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)

    المصدر: Beilstein Journal of Organic Chemistry
    Beilstein Journal of Organic Chemistry, Beilstein-Institut, 2017, 13, pp.2862-2868. ⟨10.3762/bjoc.13.278⟩
    Beilstein Journal of Organic Chemistry, 2017, 13, pp.2862-2868. ⟨10.3762/bjoc.13.278⟩
    Beilstein Journal of Organic Chemistry, Vol 13, Iss 1, Pp 2862-2868 (2017)

    مصطلحات موضوعية: chemistry.chemical_element, 010402 general chemistry, 01 natural sciences, Full Research Paper, C–H bond activation, Catalysis, lcsh:QD241-441, chemistry.chemical_compound, lcsh:Organic chemistry, [CHIM]Chemical Sciences, Reactivity (chemistry), Thiazole, lcsh:Science, catalysis, 010405 organic chemistry, Organic Chemistry, Halogenation, heteroarenes, palladium, Thiophene derivatives, Combinatorial chemistry, 0104 chemical sciences, Chemistry, C-H bond activation, chemistry, lcsh:Q, selenophene, Palladium

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::294333a3fbb5106666b3b4baf0fd4f2b
    https://hal-univ-rennes1.archives-ouvertes.fr/hal-01709524/file/1860-5397-13-278.pdf

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  9. 9
    Access to (Hetero) arylated Selenophenes via Palladium-catalysed Stille, Negishi or Suzuki Couplings or C-H Bond Functionalization Reaction

    المؤلفون: Jean-François Soulé, Aymen Skhiri, Ridha Ben Salem, Henri Doucet

    المساهمون: Institut des Sciences Chimiques de Rennes (ISCR), Université de Rennes (UR)-Institut National des Sciences Appliquées - Rennes (INSA Rennes), Institut National des Sciences Appliquées (INSA)-Institut National des Sciences Appliquées (INSA)-Ecole Nationale Supérieure de Chimie de Rennes (ENSCR)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Université de Sfax - University of Sfax, Université de Rennes 1 (UR1), Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-Institut National des Sciences Appliquées - Rennes (INSA Rennes), Institut National des Sciences Appliquées (INSA)-Université de Rennes (UNIV-RENNES)-Institut National des Sciences Appliquées (INSA)-Ecole Nationale Supérieure de Chimie de Rennes (ENSCR)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)

    المصدر: ChemCatChem
    ChemCatChem, 2017, 9 (15), pp.2895--2913. ⟨10.1002/cctc.201700256⟩
    ChemCatChem, Wiley, 2017, 9 (15), pp.2895--2913. ⟨10.1002/cctc.201700256⟩

    مصطلحات موضوعية: Coupling, C h bond, 010405 organic chemistry, Chemistry, Negishi coupling, Organic Chemistry, chemistry.chemical_element, c-h activation, [CHIM.CATA]Chemical Sciences/Catalysis, 010402 general chemistry, palladium, 01 natural sciences, Combinatorial chemistry, Catalysis, Coupling reaction, 0104 chemical sciences, Stille reaction, Inorganic Chemistry, Suzuki reaction, selenophenes, Surface modification, Physical and Theoretical Chemistry, coupling, arylated, Palladium

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c5a2f28ca578cd35a4de11c2b6f9043
    https://univ-rennes.hal.science/hal-01578539/document

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  10. 10
    Unprecedented Access to β-Arylated Selenophenes through Palladium-Catalysed Direct Arylation

    المؤلفون: Ridha Ben Salem, Aymen Skhiri, Jean-François Soulé, Henri Doucet

    المساهمون: Institut des Sciences Chimiques de Rennes (ISCR), Université de Rennes 1 (UR1), Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-Institut National des Sciences Appliquées - Rennes (INSA Rennes), Institut National des Sciences Appliquées (INSA)-Université de Rennes (UNIV-RENNES)-Institut National des Sciences Appliquées (INSA)-Ecole Nationale Supérieure de Chimie de Rennes (ENSCR)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Université de Sfax - University of Sfax, Université de Rennes (UR)-Institut National des Sciences Appliquées - Rennes (INSA Rennes), Institut National des Sciences Appliquées (INSA)-Institut National des Sciences Appliquées (INSA)-Ecole Nationale Supérieure de Chimie de Rennes (ENSCR)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)

    المصدر: Chemistry-A European Journal
    Chemistry-A European Journal, Wiley-VCH Verlag, 2017, 23 (12), pp.2788-2791. ⟨10.1002/chem.201700202⟩
    Chemistry-A European Journal, 2017, 23 (12), pp.2788-2791. ⟨10.1002/chem.201700202⟩

    مصطلحات موضوعية: Solid-state chemistry, 010405 organic chemistry, Chemistry, [CHIM.ORGA]Chemical Sciences/Organic chemistry, Aryl, Organic Chemistry, chemistry.chemical_element, General Chemistry, 010402 general chemistry, Homogeneous catalysis, palladium, 01 natural sciences, Catalysis, 0104 chemical sciences, chemistry.chemical_compound, C−H functionalization, benzenesulfonyl chlorides, Organic chemistry, Selenophenes, Benzene, Palladium

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5828d61700ff0d13ae929a593e356509
    https://hal-univ-rennes1.archives-ouvertes.fr/hal-01501260

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