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Synthesis 2012(5): 677-685
DOI: 10.1055/s-0031-1289697
DOI: 10.1055/s-0031-1289697
REVIEW
© Georg Thieme Verlag
Stuttgart ˙ New York
Transition-Metal-Catalyzed Synthesis of Aromatic Ketones via Direct C-H Bond Activation
Further Information
Received
2 November 2011
Publication Date:
13 February 2012 (online)
Publication History
Publication Date:
13 February 2012 (online)
Abstract
There are several alternative methods to Friedel-Crafts acylation for the synthesis of ketones. Among these methods, transition-metal-catalyzed acylation of arenes via C-H bond cleavage represents a direct and promising approach to access ketones, in view of the advantages of C-H bond activation; recent advances in the development of this area are summarized.
1 Introduction
2 Acylation of sp² C-H Bonds with Aldehydes via C-H Bond Cleavage
3 Acylation of Arenes with α-Oxocarboxylic Acids via Decarboxylation and C-H Bond Cleavage
4 Acylation of sp² C-H Bonds with α,β-Unsaturated Carboxylic Acids
5 Acylation of sp² C-H Bonds with Acyl Chlorides
6 Summary
Key words
acylation - transition metals - arenes - ketones - C-H bond functionalization
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