Abstract
Transition-metal-catalyzed oxidative and decarboxylative acylations of sp2 C-H bonds bearing conventional directing groups with various acyl equivalents, such as aldehydes, alcohols, alkylbezenes, -keto acids, etc. are described. These protocols present an effective and promising route to obtain aryl ketones, which are found to be important precursors for the formation of bioactive molecules and functional materials. Thus, oxidative and decarboxylative C-H acylations potentially provide a catalytic alternative to overcome the limitations of classical Friedel-Crafts acylation. This review is intended to give an overview on recent advances on catalytic acylation reactions through C-H bond activation.
Keywords: Acylation, catalytic, decarboxylative, oxidative, transition metal.
Graphical Abstract
Current Organic Chemistry
Title:Transition-Metal-Catalyzed Oxidative and Decarboxylative Acylations through sp2 C-H Bond Activation
Volume: 20 Issue: 5
Author(s): Satyasheel Sharma, Neeraj Kumar Mishra, Youngmi Shin and In Su Kim
Affiliation:
Keywords: Acylation, catalytic, decarboxylative, oxidative, transition metal.
Abstract: Transition-metal-catalyzed oxidative and decarboxylative acylations of sp2 C-H bonds bearing conventional directing groups with various acyl equivalents, such as aldehydes, alcohols, alkylbezenes, -keto acids, etc. are described. These protocols present an effective and promising route to obtain aryl ketones, which are found to be important precursors for the formation of bioactive molecules and functional materials. Thus, oxidative and decarboxylative C-H acylations potentially provide a catalytic alternative to overcome the limitations of classical Friedel-Crafts acylation. This review is intended to give an overview on recent advances on catalytic acylation reactions through C-H bond activation.
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Cite this article as:
Sharma Satyasheel, Kumar Mishra Neeraj, Shin Youngmi and Su Kim In, Transition-Metal-Catalyzed Oxidative and Decarboxylative Acylations through sp2 C-H Bond Activation, Current Organic Chemistry 2016; 20 (5) . https://dx.doi.org/10.2174/1385272819666150122234834
DOI https://dx.doi.org/10.2174/1385272819666150122234834 |
Print ISSN 1385-2728 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5348 |
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