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      Organocatalytic Diastereo- and Enantioselective 1,3-Dipolar Cycloaddition of Azlactones and Methyleneindolinones

      , , , , ,
      Angewandte Chemie International Edition
      Wiley-Blackwell

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          Pyrrolidinyl-spirooxindole natural products as inspirations for the development of potential therapeutic agents.

          The 3,3'-pyrrolidinyl-spirooxindole unit is a privileged heterocyclic motif that forms the core of a large family of alkaloid natural products with strong bioactivity profiles and interesting structural properties. Significant recent advances in the synthesis of this fused heterocyclic system have led to intense interest in the development of related compounds as potential medicinal agents or biological probes.
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            Catalytic Asymmetric Synthesis of Oxindoles Bearing a Tetrasubstituted Stereocenter at the C-3 Position

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              Construction of Spiro[pyrrolidine-3,3′-oxindoles] − Recent Applications to the Synthesis of Oxindole Alkaloids

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                Author and article information

                Journal
                Angewandte Chemie International Edition
                Angew. Chem. Int. Ed.
                Wiley-Blackwell
                14337851
                August 12 2013
                August 12 2013
                : 52
                : 33
                : 8633-8637
                Article
                10.1002/anie.201302831
                2ab18a9c-6144-42bf-9d41-572621e46a6a
                © 2013

                http://doi.wiley.com/10.1002/tdm_license_1.1

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