Titlebook: Ni- and Fe-Based Cross-Coupling Reactions; Arkaitz Correa Book 2017 The Editor(s) (if applicable) and The Author(s), under exclusive licen

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https://doi.org/10.1007/978-3-319-49784-6C-C Couplings; Alkyl Electrophiles; Ni-Catalyzed Carboxylations; Phenolic Electrophiles; C-H Functionali

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Arthropathy

Ni- and Fe-Based Cross-Coupling Reactions978-3-319-49784-6Series ISSN 2367-4067 Series E-ISSN 2367-4075

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,Ni-Catalyzed C–C Couplings Using Alkyl Electrophiles,eagents, and significant achievements in this area have emerged during the past two decades. Nickel catalysts have enabled the coupling reaction of not only primary alkyl electrophiles, but also sterically hindered secondary and tertiary alkyl electrophiles possessing b-hydrogens with various organo

AXIS

Photoredox Catalysis in Nickel-Catalyzed Cross-Coupling,ward coupling of C(sp3)-hybridized centers, particularly using functional group tolerant reagents and reaction conditions. The development of photoredox/Ni dual catalytic methods for cross-coupling has opened new vistas for the construction of carbon–carbon bonds at C(sp3)-hybridized centers. In thi

conspicuous

異常

Ni- and Fe-catalyzed Carboxylation of Unsaturated Hydrocarbons with CO2,ic synthesis. In this regard, the implementation of abundant and inexpensive carbon dioxide (CO.) as a C1 building block has recently attracted considerable attention. Among the different alternatives in CO. fixation, the preparation of carboxylic acids, relevant motifs in pharmaceuticals and agroch

observatory

,Nickel-Catalyzed Cross-Coupling Reactions of Unreactive Phenolic Electrophiles via C–O Bond Activat derivatives cannot be activated by palladium, a typical cross-coupling catalyst, but a low valent nickel species in conjunction with a strong r-donor ligand is uniquely effective for achieving this. The review is organized primarily by substrate class and secondarily by coupling partners, encompass