يعرض 1 - 10 نتائج من 112 نتيجة بحث عن '"Ange Pancrazi"', وقت الاستعلام: 1.13s تنقيح النتائج
  1. 1
    Total Synthesis of Discodermolide: Optimization of the Effective Synthetic Route

    المؤلفون: Evangelos Agouridas, Elsa De Lemos, Arnaud Bourin, Janick Ardisson, Julien Barbion, Alain Commerçon, Marie-Isabelle Lannou, Jean-François Betzer, François-Hugues Porée, Ange Pancrazi

    المساهمون: Les Laboratoires Biodim-Mutabilis, Biocitech, Institut de Chimie des Substances Naturelles (ICSN), Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC), Synthèse Organique Sélective et Chimie Organométallique (SOSCO), Université de Cergy Pontoise (UCP), Université Paris-Seine-Université Paris-Seine-ESCOM-Centre National de la Recherche Scientifique (CNRS), Chimie Organique, Médicinale et Extractive et Toxicologie Expérimentale (COMETE - UMR 8638), Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université Paris Descartes - Paris 5 (UPD5), Synthèse et électrosynthèse organiques (SESO), Université de Rennes 1 (UR1), Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-Centre National de la Recherche Scientifique (CNRS), Centre National de la Recherche Scientifique (CNRS), Centre National de la Recherche Scientifique (CNRS)-ESCOM-Université de Cergy Pontoise (UCP), Université Paris-Seine-Université Paris-Seine, Université Paris Descartes - Paris 5 (UPD5)-Centre National de la Recherche Scientifique (CNRS)

    المصدر: Chemistry-A European Journal
    Chemistry-A European Journal, Wiley-VCH Verlag, 2008, 14 (35), pp.11092-11112. ⟨10.1002/chem.200801478⟩

    مصطلحات موضوعية: Diene, Stereochemistry, Antineoplastic Agents, Alkenes, 010402 general chemistry, 01 natural sciences, Catalysis, Lactones, chemistry.chemical_compound, Polyketide, Alkanes, Moiety, ComputingMilieux_MISCELLANEOUS, [CHIM.ORGA]Chemical Sciences/Organic chemistry, 010405 organic chemistry, Chemistry, Organic Chemistry, Total synthesis, General Chemistry, Discodermolide, Highly selective, Combinatorial chemistry, Tubulin Modulators, 0104 chemical sciences, Pyrones, Alcohols, Yield (chemistry), Carbamates, Selectivity

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::589a61425d39a647e2613f36c8dc73dc
    https://doi.org/10.1002/chem.200801478

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  2. 2
    Total Synthesis of Rhizoxin D

    المؤلفون: Nathalie Lensen, Janick Ardisson, Marie‐Ange N'Zoutani, Ange Pancrazi

    المصدر: Synlett. :491-495

    مصطلحات موضوعية: chemistry.chemical_classification, chemistry.chemical_compound, Rhizoxin D, chemistry, Double bond, Stereochemistry, Heck reaction, Organic Chemistry, Side chain, Total synthesis, Enone, Aldehyde, Derivative (chemistry)

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::19abc4d3d9a041f06b3b50bc09721996
    https://doi.org/10.1055/s-2005-862373

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  3. 3
    Primary and Secondary Allyltitanium(IV) Reagents in Aldehyde Allylation II: Application to an Enantioselective Preparation of a C1-C7 Fragment of Spiramycin

    المؤلفون: Marie‐Ange N'Zoutani, Ange Pancrazi, Janick Ardisson, Patrick Razon, Sylvie Dhulut, Sophie Bezzenine‐Lafollee

    المصدر: Synthesis. 2005:109-121

    مصطلحات موضوعية: chemistry.chemical_classification, Carbamate, Chemistry, medicine.medical_treatment, Organic Chemistry, Spiramycin, Enantioselective synthesis, Medicinal chemistry, Aldehyde, Catalysis, Kinetic resolution, Reagent, Yield (chemistry), medicine, Side chain, medicine.drug

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::7f05f159c355dbbecf578a2618a676b8
    https://doi.org/10.1055/s-2004-834913

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  4. 4
    Secondary Allyltitanium(IV) Reagents in Aldehyde Allylation I: Extension of the Hoppe Reaction to γ-Alkoxy Secondary Allyl Carbamates

    المؤلفون: Patrick Razon, Sylvie Dhulut, Sophie Bezzenine‐Lafollee, Janick Ardisson, Jacques Courtieu, Ange Pancrazi

    المصدر: Synthesis. 2005:102-108

    مصطلحات موضوعية: chemistry.chemical_classification, chemistry, Deuterium, Reagent, Yield (chemistry), Organic Chemistry, Alkoxy group, Enantiomer, Optically active, Enantiomeric excess, Aldehyde, Medicinal chemistry, Catalysis

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::3bf834bcd407c99329de7ba503c1ac5f
    https://doi.org/10.1055/s-2004-834912

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  5. 5
    Zinc-Acetic Acid Reductive Cyclisation in a Two-Step Synthesis of the S1-N10 Nine-Membered Lactone Core ofent-Griseoviridin

    المؤلفون: Janick Ardisson, Grégory Chaume, Louis Ricard, Carine Kuligowski, Ange Pancrazi, Sophie Bezzenine-Laffolée

    المصدر: Synthesis. :3029-3036

    مصطلحات موضوعية: chemistry.chemical_classification, Stereochemistry, Organic Chemistry, Cystine, chemistry.chemical_element, Zinc, Catalysis, Acetic acid, chemistry.chemical_compound, Griseoviridin, chemistry, Yield (chemistry), Moiety, Lactone, Derivative (chemistry)

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::36b3a5620ed316ab0900f763b7b4be67
    https://doi.org/10.1055/s-2004-834899

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  6. 6
    Efficient preparation of (Z)-alkenyl derivatives from (Z)-vinyl (N,N-diisopropyl)carbamate via Ni-catalysed coupling reactions

    المؤلفون: Alexandre Clavel, Ange Pancrazi, François-Hugues Porée, Janick Ardisson, Jean-François Betzer

    المساهمون: Institut de Chimie des Substances Naturelles (ICSN), Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)

    المصدر: Tetrahedron Letters
    Tetrahedron Letters, Elsevier, 2003, 44 (40), pp.7553-7556. ⟨10.1016/S0040-4039(03)01804-5⟩

    مصطلحات موضوعية: Carbamate, [CHIM.ORGA]Chemical Sciences/Organic chemistry, 010405 organic chemistry, Chemistry, medicine.medical_treatment, Organic Chemistry, General Medicine, macromolecular substances, Grignard reagent, 010402 general chemistry, 01 natural sciences, Biochemistry, Chloride, Medicinal chemistry, Coupling reaction, Catalysis, 3. Good health, 0104 chemical sciences, chemistry.chemical_compound, Bromide, Reagent, Drug Discovery, medicine, Organic chemistry, medicine.drug

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::736e62aaa0886a527457b5268f91b940
    https://doi.org/10.1016/s0040-4039(03)01804-5

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  7. 7
    IMDA reaction in a synthetic approach towards a natural kijamicin aglycon analog

    المؤلفون: Jean-François Betzer, Ange Pancrazi, Janick Ardisson

    المصدر: Comptes Rendus de l'Académie des Sciences - Series IIC - Chemistry. 4:695-704

    مصطلحات موضوعية: chemistry.chemical_classification, Intramolecular reaction, Bicyclic molecule, Stereochemistry, chemistry.chemical_element, General Chemistry, Aldehyde, Chemical synthesis, Catalysis, Stille reaction, chemistry.chemical_compound, Aglycone, chemistry, Palladium

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::c77971098549571f709ad847387c998b
    https://doi.org/10.1016/s1387-1609(01)01260-9

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  8. 8
    Stereospecific Preparation of Silyldienes - Electrophilic Substitution as an Access to Dienones

    المؤلفون: Patrick Le Menez, Marie Elise Tran Huu Dau, Isabelle Berque, Valérie Fargeas, Janick Ardisson, Ange Pancrazi

    المصدر: Synlett. 1996:1125-1128

    مصطلحات موضوعية: Electrophilic substitution, chemistry.chemical_compound, Stereospecificity, chemistry, Stereochemistry, Organic Chemistry, Tylosin

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::0bb94e3872c2b495b3c6f5781541c69c
    https://doi.org/10.1055/s-1996-5660

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  9. 9
    Alkyne Zip Reaction in the Synthesis of a Taxoid C-Ring

    المؤلفون: Thierry Prangé, Damien Bourgeois, Jean-Yves Lallemand, Joëlle Prunet, Ange Pancrazi

    المساهمون: Laboratoire de synthèse organique (DCSO), École polytechnique (X)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Synthèse Organique Sélective et Chimie Organométallique (SOSCO), Université de Cergy Pontoise (UCP), Université Paris-Seine-Université Paris-Seine-ESCOM-Centre National de la Recherche Scientifique (CNRS), Laboratoire de Chimie Structurale Biomoléculaire

    المصدر: European Journal of Organic Chemistry
    European Journal of Organic Chemistry, Wiley-VCH Verlag, 2000, pp.4029-4036. ⟨10.1002/1099-0690(200012)2000:243.0.CO;2-0⟩
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    مصطلحات موضوعية: chemistry.chemical_classification, Taxoid, Diketone, chemistry, Stereochemistry, Organic Chemistry, Enantioselective synthesis, Alkyne, Total synthesis, Hydrazone, Physical and Theoretical Chemistry, Triple bond, Isomerization

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fec88a816a81495a02e7841e5cc8692d
    https://doi.org/10.1002/1099-0690(200012)2000:24<4029::aid-ejoc4029>3.0.co;2-0

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  10. 10
    Synthesis of Highly Functionalized Cyclooctenes by Ring-Closing Metathesis: Unexpected Formation of atrans Isomer

    المؤلفون: Damien Bourgeois, Louis Ricard, Joëlle Prunet, Ange Pancrazi

    المساهمون: Laboratoire de synthèse organique (DCSO), École polytechnique (X)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Laboratoire de Synthèse Organique Sélective et Chimiie Organométallique, affiliation inconnue, Laboratoire Hétéroéléments et Coordination (DCPH)

    المصدر: Angewandte Chemie International Edition
    Angewandte Chemie International Edition, Wiley-VCH Verlag, 2000, 39 (4), pp.725-728. ⟨10.1002/(SICI)1521-3773(20000218)39:43.0.CO;2-I⟩

    مصطلحات موضوعية: chemistry.chemical_classification, Alkene, Stereochemistry, [CHIM.ORGA]Chemical Sciences/Organic chemistry, General Chemistry, General Medicine, Metathesis, Catalysis, chemistry.chemical_compound, Ring-closing metathesis, chemistry, Cyclooctene, Ring-opening metathesis polymerisation, Cis–trans isomerism, Acyclic diene metathesis

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::053cfb592edf5631b3bab163c89adb21
    https://doi.org/10.1002/(sici)1521-3757(20000218)112:4<741::aid-ange741>3.0.co;2-j

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