Catalytic C-H to C-M (M = Al, Mg) bond transformations with heterometallic complexes
C-H functionalisation is one of the cornerstones of modern catalysis and remains a topic of contemporary interest due its high efficiency and atom-economy. Among these reactions, C-H borylation, that is the transformation of C-H to C-B bonds, has experienced a fast development because of the wide ut...
Gespeichert in:
Veröffentlicht in: | Chemical science (Cambridge) 2020-08, Vol.12 (6), p.1993-2 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | C-H functionalisation is one of the cornerstones of modern catalysis and remains a topic of contemporary interest due its high efficiency and atom-economy. Among these reactions, C-H borylation, that is the transformation of C-H to C-B bonds, has experienced a fast development because of the wide utility of organoboron reagents as synthetic intermediates. The mechanistic background is now well-understood and the role of transition metal boryl or σ-borane intermediates in this transformation is well documented. This mini-review focuses on efforts made by our group, and others, to establish palladium- and calcium-catalysed methods for C-H metalation employing heavier main group elements (M = Al, Mg). These are new catalytic reactions first accomplished in our group that we have termed C-H alumination and magnesiation respectively. Unusual heterometallic complexes have been identified as key on-cycle intermediates and their unique reactivity is discussed in the context of new catalytic pathways for C-H functionalisation. Hence, this mini-review summarises the recent progress in the area of C-H metalation reactions as well as the new opportunities that may arise from this concept.
This highlight focuses on recent efforts to establish catalytic methods for C-H functionalisation with main group metals (M = Al, Mg). |
---|---|
ISSN: | 2041-6520 2041-6539 |
DOI: | 10.1039/d0sc03695a |