Giorgio Giorgi Poletti-rekin lankidetzan egindako argitalpenak (11)

2017

  1. A systematic 1H- and 13C-NMR spectral analysis of bicyclo[n.3.1]alkanone systems: Determination of the relative configuration of the stereogenic centres and conformation of the six-membered ring

    Magnetic Resonance in Chemistry

  2. Empleo del Campus Virtual en docencia práctica: una herramienta para una enseñanza universitaria en inglés e inclusiva

    Enseñanza de las ciencias: revista de investigación y experiencias didácticas, Núm. 0, pp. 1801-1806

2013

  1. Michael additions in aqueous media: "on-water" and "in-water" processes from α-nitro ketones and their anions

    European Journal of Organic Chemistry, pp. 1327-1336

2012

  1. A one-pot sequence for the efficient synthesis of highly functionalized macrocarbocycles or bridged 2,8-dioxabicyclo[3.2.1]octanes from 1-nitrobicyclic compounds

    Organic and Biomolecular Chemistry, Vol. 10, Núm. 26, pp. 5131-5136

2011

  1. A general, diastereoselective synthesis of highly functionalized bicyclo[n.3.1]alkane systems based on an anionic domino reaction of α-nitrocycloalkanones

    European Journal of Organic Chemistry, pp. 2101-2110

  2. Domino reactions for the synthesis of bridged bicyclic frameworks: Fast access to bicyclo[n.3.1]alkanes

    Chemical Society Reviews, Vol. 40, Núm. 7, pp. 3445-3454

  3. Synthesis of benzo- and naphtho-fused bicyclo[n.3.1]alkane frameworks with a bridgehead nitrogen function by palladium-catalyzed intramolecular α′-arylation of α-nitroketones

    Organic and Biomolecular Chemistry, Vol. 9, Núm. 8, pp. 2722-2730

  4. Two chemodivergent anionic domino processes from cyclic α-nitroketones and aromatic aldehydes

    Tetrahedron, Vol. 67, Núm. 31, pp. 5582-5589

2010

  1. Three-component, diastereoselective synthesis of highly functionalized indane derivatives based on an anionic domino sequence from α-nitroketones

    Synlett, pp. 2465-2467

2005

  1. Unique michael addition-initiated domino reaction for the stereoselective synthesis of functionalized macrolactones from α-nitroketones in water

    Organic Letters, Vol. 7, Núm. 11, pp. 2197-2200

2003

  1. Practical and User-Friendly Procedure for Michael Reactions of α-Nitroketones in Water

    Synlett, pp. 2159-2162