Journal
CHEMICAL SOCIETY REVIEWS
Volume 51, Issue 17, Pages 7358-7426Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d1cs00923k
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Funding
- SERB TETRA [TTR/2021/000108]
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Transition metal catalysis has played an important role in C-C bond formation reactions, including alkylation. Compared to traditional methods, transition metal catalysis offers advantages such as fewer reaction steps, shorter reaction times, atom economy, and control over regio- and stereo-selectivity. The hydrocarbonation of alkenes has received increased attention due to its ability to selectively synthesize various industrially and pharmaceutically relevant compounds. This review provides a scientific and systematic analysis of recent developments in transition metal-catalyzed alkylation of C-H bonds using simple and activated olefins, highlighting key features and mechanistic studies.
Transition metal catalysis has contributed immensely to C-C bond formation reactions over the last few decades, and alkylation is no exception. The superiority of such methodologies over traditional alkylation is evident from minimal reaction steps, shorter reaction times, and atom economy while also allowing control over regio- and stereo-selectivity. In particular, hydrocarbonation of alkenes has grabbed increased attention due its fundamental ability to effectively and selectively synthesise a wide range of industrially and pharmaceutically relevant moieties. This review attempts to provide a scientific viewpoint and a systematic analysis of the recent developments in transition-metal-catalyzed alkylation of various C-H bonds using simple and activated olefins. The key features and mechanistic studies involved in these transformations are described briefly.
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