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      Enantioselective [3 + 2] annulation via C–H activation between cyclic N-acyl ketimines and 1,3-dienes catalyzed by iridium/chiral diene complexes

      , , ,
      Chemical Science
      Royal Society of Chemistry (RSC)

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          Palladium(II)-catalyzed C-H activation/C-C cross-coupling reactions: versatility and practicality.

          In the past decade, palladium-catalyzed C-H activation/C-C bond-forming reactions have emerged as promising new catalytic transformations; however, development in this field is still at an early stage compared to the state of the art in cross-coupling reactions using aryl and alkyl halides. This Review begins with a brief introduction of four extensively investigated modes of catalysis for forming C-C bonds from C-H bonds: Pd(II)/Pd(0), Pd(II)/Pd(IV), Pd(0)/Pd(II)/Pd(IV), and Pd(0)/Pd(II) catalysis. A more detailed discussion is then directed towards the recent development of palladium(II)-catalyzed coupling of C-H bonds with organometallic reagents through a Pd(II)/Pd(0) catalytic cycle. Despite the progress made to date, improving the versatility and practicality of this new reaction remains a tremendous challenge.
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            Rhodium-catalyzed C-C bond formation via heteroatom-directed C-H bond activation.

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              Carboxylate-assisted transition-metal-catalyzed C-H bond functionalizations: mechanism and scope.

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                Author and article information

                Journal
                CSHCBM
                Chemical Science
                Chem. Sci.
                Royal Society of Chemistry (RSC)
                2041-6520
                2041-6539
                2013
                2013
                : 4
                : 12
                : 4499
                Article
                10.1039/c3sc52379a
                9d410664-023e-401f-a816-e6f43de1f0ee
                © 2013
                History

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