Palladium-Catalyzed Transformations of Alkyl C-H Bonds.

Chem Rev

Department of Chemistry, The Scripps Research Institute, 10550 N. Torrey Pines Road, La Jolla, California 92037, United States.

Published: July 2017

This Review summarizes the advancements in Pd-catalyzed C(sp)-H activation via various redox manifolds, including Pd(0)/Pd(II), Pd(II)/Pd(IV), and Pd(II)/Pd(0). While few examples have been reported in the activation of alkane C-H bonds, many C(sp)-H activation/C-C and C-heteroatom bond forming reactions have been developed by the use of directing group strategies to control regioselectivity and build structural patterns for synthetic chemistry. A number of mono- and bidentate ligands have also proven to be effective for accelerating C(sp)-H activation directed by weakly coordinating auxiliaries, which provides great opportunities to control reactivity and selectivity (including enantioselectivity) in Pd-catalyzed C-H functionalization reactions.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5516964PMC
http://dx.doi.org/10.1021/acs.chemrev.6b00622DOI Listing

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