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DerechosPreviewFecha Public.TítuloAutor(es)Tipo
1closedAccessjul-1995Free radical cycloisomerization of enantiomerically pure alkyne-tethered oxime ethers: A new method for the asymmetric synthesis of aminocyclopentitolsMarco-Contelles, José CSIC ORCID; Destabel, Christine; Chiara, José Luis CSIC ORCID ; Bernabé, Manuel CSICartículo
2openAccessjo00124a007.pdf.jpgsep-1995Intramolecular reductive coupling of carbonyl-tethered oxime ethers promoted by samarium diiodide: A powerful method for the stereoselective synthesis of aminocyclopentitolsChiara, José Luis CSIC ORCID ; Marco-Contelles, José CSIC ORCID; Khiar el Wahabi, Noureddine CSIC ORCID; Gallego, Pilar; Destabel, Christine; Bernabé, Manuel CSICartículo
3closedAccess1996Palladium-catalyzed reduction of a propargylic acetate derived from a sugar with SmI2. Some unexpectedMarco-Contelles, José CSIC ORCID; Destabel, Christine; Chiara, José Luis CSIC ORCID artículo
4openAccessjo951571q.pdf.jpg12-ene-1996Cleavage of N−O Bonds Promoted by Samarium Diiodide: Reduction of Free or N-Acylated O-AlkylhydroxylaminesChiara, José Luis CSIC ORCID ; Destabel, Christine; Gallego, Pilar; Marco-Contelles, José CSIC ORCIDartículo
5openAccessjo951891%2B.pdf.jpgfeb-1996A New Synthetic Approach to the Carbocyclic Core of Cyclopentane-Type Glycosidase Inhibitors: Asymmetric Synthesis of Aminocyclopentitols via Free Radical Cycloisomerization of Enantiomerically Pure Alkyne- Tethered Oxime Ethers Derived from CarbohydratesMarco-Contelles, José CSIC ORCID; Destabel, Christine; Gallego, Pilar; Chiara, José Luis CSIC ORCID ; Bernabé, Manuel CSICartículo
6openAccessjo970987w.pdf.jpg17-oct-1997Synthesis of Aminocyclitols by Intramolecular Reductive Coupling of Carbohydrate Derived δ- and ε-Functionalized Oxime Ethers Promoted by Tributyltin Hydride or Samarium DiiodideMarco-Contelles, José CSIC ORCID; Gallego, Pilar; Rodríguez-Fernández, Mercedes; Khiar el Wahabi, Noureddine CSIC ORCID; Destabel, Christine; Bernabé, Manuel CSIC; Martínez-Grau, Angeles; Chiara, José Luis CSIC ORCID artículo

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