Mild metal-catalyzed C–H activation: examples and concepts
T. Gensch, M. N. Hopkinson, F. Glorius, and J. Wencel-Delord
Chem. Soc. Rev.
Abstract:
Organic reactions that involve the direct
functionalization of non-activated C–H bonds represent an attractive
class of transformations which maximize atom- and step-economy, and
simplify chemical synthesis. Due to the high stability of C–H bonds,
these processes, however, have most often required harsh reaction
conditions, which has drastically limited their use as tools for the
synthesis of complex organic molecules. Following the increased
understanding of mechanistic aspects of C–H activation gained over
recent years, great strides have been taken to design and develop new
protocols that proceed efficiently under mild conditions and duly
benefit from improved functional group tolerance and selectivity. In
this review, we present the current state of the art in this field and
detail C–H activation transformations reported since 2011 that proceed
either at or below ambient temperature, in the absence of strongly
acidic or basic additives or without strong oxidants. Furthermore, by
identifying and discussing the major strategies that have led to these
improvements, we hope that this review will serve as a useful conceptual
overview and inspire the next generation of mild C–H transformations.
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