Chemical Society Reviews· 2016Q1· Review
Mild metal-catalyzed C–H activation: examples and concepts
- 1,770citations
- Q1SCImago
- 2016year
Short summary
Metal-catalyzed C–H activation reactions now proceed efficiently under mild conditions (ambient temperature, no strong additives/oxidants), enabling more atom- and step-economical synthesis of complex molecules.
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Key points
- Mild C–H activation protocols now exist, operating at or below ambient temperature.
- These reactions avoid harsh conditions like strong acids, bases, or oxidants.
- Mild conditions improve functional group tolerance and selectivity.
- This approach maximizes atom- and step-economy in chemical synthesis.
AI-generated from the title and abstract; the full text is not read.
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.
The authors' abstract, as published at the source. Chemical Society Reviews, 2016 · DOI ↗
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Field: Organic Chemistry
Organic ChemistryChemistry