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Transition‐Metal‐Catalyzed C−H Bond Functionalization of Arenes/Heteroarenes via Tandem C−H Activation and Subsequent Carbene Migratory Insertion Strategy.
- Source :
- Chemical Record; Dec2021, Vol. 21 Issue 12, p4088-4122, 35p
- Publication Year :
- 2021
-
Abstract
- The past decade has witnessed tremendous developments in transition‐metal‐catalyzed C−H bond activation and subsequent carbene migratory insertion reactions, thus assisting in the construction of diverse arene/heteroarene scaffolds. Various transition‐metal catalysts serve this purpose and provide efficient pathways for an easy access to substituted heterocycles. A brief introduction to metal‐carbenes has been provided along with key mechanistic pathways underlying the coupling reactions. The purpose of this review is to provide a concise knowledge about diverse directing group‐assisted coupling of varied arenes/heteroarenes and acceptor‐acceptor/donor‐acceptor diazo compounds. The review also highlights the synthesis of various carbocycles and fused heterocycles through diazo insertion pathways, via C−C, C−N and C−O bond forming reactions. The mechanism usually involves a C−H activation process, followed by diazo insertion leading to subsequent coupling. [ABSTRACT FROM AUTHOR]
- Subjects :
- HETEROARENES
AROMATIC compounds
HETEROCYCLIC compounds
DIAZO compounds
Subjects
Details
- Language :
- English
- ISSN :
- 15278999
- Volume :
- 21
- Issue :
- 12
- Database :
- Complementary Index
- Journal :
- Chemical Record
- Publication Type :
- Academic Journal
- Accession number :
- 154347882
- Full Text :
- https://doi.org/10.1002/tcr.202100193