Direct functionalization of unactivated C-H bonds catalyzed by group 3-5 metal alkyl complexes
This perspective summarizes direct C-H bond functionalization reactions catalyzed by group 3-5 metal alkyl complexes. Metal-carbon bonds of group 3-5 metals have potentially high reactivity toward both C-H bond activation reactions through the intrinsic σ-bond metathesis pathway and insertion of uns...
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Veröffentlicht in: | Dalton transactions : an international journal of inorganic chemistry 2014-01, Vol.43 (6), p.2331-2343 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | This perspective summarizes direct C-H bond functionalization reactions catalyzed by group 3-5 metal alkyl complexes. Metal-carbon bonds of group 3-5 metals have potentially high reactivity toward both C-H bond activation reactions through the intrinsic σ-bond metathesis pathway and insertion of unsaturated organic molecules. Upon the combination of these two elemental steps, direct C-H bond functionalization reactions of (hetero)aromatic compounds, methane, alkylamines, and terminal alkynes, proceed through C(sp)-H, C(sp
2
)-H, and C(sp
3
)-H bond activation reactions. Here we review as catalysts for these transformations not only simple metallocene complexes but also non-metallocene complexes supported by a variety of ligands, which are often superior in terms of catalyst design and catalytic activity.
We reviewed recent achievements in catalytic C-C and C-Si bond forming reactions through C-H bond activation by group 3-5 metal complexes. |
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ISSN: | 1477-9226 1477-9234 |
DOI: | 10.1039/c3dt52758a |