Academic Journal
Synthesis of Unnatural Phosphonosugar Analogues.
العنوان: | Synthesis of Unnatural Phosphonosugar Analogues. |
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المؤلفون: | Dayde, Bénédicte, Pierra, Claire, Gosselin, Gilles, Surleraux, Dominique, Tidjani Ilagouma, Amadou, Laborde, Coralie, Volle, Jean-Noël, Virieux, David, Pirat, Jean-Luc |
المساهمون: | Idenix Pharmaceuticals, Medicinal Chemistry Laboratory-Cap Gamma, Institut Charles Gerhardt Montpellier - Institut de Chimie Moléculaire et des Matériaux de Montpellier (ICGM ICMMM), Université Montpellier 1 (UM1)-Université Montpellier 2 - Sciences et Techniques (UM2)-Ecole Nationale Supérieure de Chimie de Montpellier (ENSCM)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS), Institut des Biomolécules Max Mousseron Pôle Chimie Balard (IBMM), Ecole Nationale Supérieure de Chimie de Montpellier (ENSCM)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS), Departement de Chimie, Abdou Moumouni University of Niamey = Université Abdou Moumouni de Niamey (UAM) |
المصدر: | ISSN: 1434-193X. |
بيانات النشر: | HAL CCSD Wiley-VCH Verlag |
سنة النشر: | 2014 |
المجموعة: | Université de Montpellier: HAL |
مصطلحات موضوعية: | Medicinal chemistry, Glycomimetics, Bioisosteres, Carbohydrates, Phosphorus heterocycles, [CHIM.ORGA]Chemical Sciences/Organic chemistry |
الوصف: | International audience ; The first synthesis of new cyclic phosphonates (phostones), analogues of pentafuranoses containing a phosphorus atom in place of the anomeric carbon in the deoxyribose and deoxyxylose series, is described. Two methods, of respectively six and seven steps, were developed in parallel, and each gave the racemic phosphonosugars in good yields. Compounds analogous to the alpha and beta anomers were isolated and fully characterized by NMR spectroscopy. |
نوع الوثيقة: | article in journal/newspaper |
اللغة: | English |
Relation: | hal-01004217; https://hal.science/hal-01004217 |
DOI: | 10.1002/ejoc.201301543 |
الاتاحة: | https://hal.science/hal-01004217 https://doi.org/10.1002/ejoc.201301543 |
رقم الانضمام: | edsbas.AEF32862 |
قاعدة البيانات: | BASE |
DOI: | 10.1002/ejoc.201301543 |
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