Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/16859
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Title: Palladium(II)-catalyzed othro-C-H-benzoxylation of 2-arylpyridines by oxidative coupling with aryl acylperoxides
Authors: Sit, WN
Chan, CW
Yu, WY 
Issue Date: 2013
Source: Molecules, Apr. 2013, v. 18, no. 4, p. 4403-4418
Abstract: A palladium(II)-catalyzed ortho-benzoxylation of 2-arylpyridines with aryl acylperoxides was developed. With pyridyl as directing group, the benzoxylation reaction exhibits remarkable regioselectivity and excellent functional group tolerance, providing the products in up to 87% yield.
Keywords: C-H bond
Oxidation
Palladium
Publisher: Mdpi Ag
Journal: Molecules 
ISSN: 1420-3049
DOI: 10.3390/molecules18044403
Rights: © 2013 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
The following publication Sit, W.-N.; Chan, C.-W.; Yu, W.-Y. Palladium(II)-Catalyzed othro-C–H-Benzoxylation of 2-Arylpyridines by Oxidative Coupling with Aryl Acylperoxides. Molecules 2013, 18, 4403-4418 is available at https://dx.doi.org/10.3390/molecules18044403
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