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CH Bond Functionalization through Intramolecular Hydride Transfer
Known for over a century, reactions that involve intramolecular hydride‐transfer events have experienced a recent resurgence. Undoubtedly responsible for the increased interest in this research area is the realization that hydride shifts represent an attractive avenue for CH bond functionalization....
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Published in: | Angewandte Chemie International Edition 2014-05, Vol.53 (20), p.5010-5036 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Known for over a century, reactions that involve intramolecular hydride‐transfer events have experienced a recent resurgence. Undoubtedly responsible for the increased interest in this research area is the realization that hydride shifts represent an attractive avenue for CH bond functionalization. The redox‐neutral nature of these complexity‐enhancing transformations makes them ideal for sustainable reaction development. This Review summarizes recent progress in this field while highlighting key historical contributions.
Known for over a century, reactions based on intramolecular hydride transfer have experienced a recent resurgence. Hydride shifts represent an attractive avenue for CH bond functionalization and the redox‐neutral nature of these transformations makes them ideal for the development of sustainable reactions. This Review summarizes recent progress in this field and highlights key historical contributions. |
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ISSN: | 1433-7851 1521-3773 |
DOI: | 10.1002/anie.201306489 |