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      Enantioselektive Katalyse photochemischer Reaktionen

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      Angewandte Chemie

      Wiley

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          Visible light photoredox catalysis with transition metal complexes: applications in organic synthesis.

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            Visible light photoredox catalysis: applications in organic synthesis.

            The use of visible light sensitization as a means to initiate organic reactions is attractive due to the lack of visible light absorbance by organic compounds, reducing side reactions often associated with photochemical reactions conducted with high energy UV light. This tutorial review provides a historical overview of visible light photoredox catalysis in organic synthesis along with recent examples which underscore its vast potential to initiate organic transformations.
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              Merging photoredox catalysis with organocatalysis: the direct asymmetric alkylation of aldehydes.

              Photoredox catalysis and organocatalysis represent two powerful fields of molecule activation that have found widespread application in the areas of inorganic and organic chemistry, respectively. We merged these two catalysis fields to solve problems in asymmetric chemical synthesis. Specifically, the enantioselective intermolecular alpha-alkylation of aldehydes has been accomplished using an interwoven activation pathway that combines both the photoredox catalyst Ru(bpy)3Cl2 (where bpy is 2,2'-bipyridine) and an imidazolidinone organocatalyst. This broadly applicable, yet previously elusive, alkylation reaction is now highly enantioselective and operationally trivial.
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                Author and article information

                Journal
                Angewandte Chemie
                Angew. Chem.
                Wiley
                00448249
                March 23 2015
                March 23 2015
                February 27 2015
                : 127
                : 13
                : 3944-3963
                Article
                10.1002/ange.201411409
                © 2015
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