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Synlett 2015; 26(20): 2843-2848
DOI: 10.1055/s-0035-1560637
DOI: 10.1055/s-0035-1560637
letter
Palladium-Catalyzed Regioselective C–H Bond Acetoxylation–Alkoxylation of Azoxybenzenes
Further Information
Publication History
Received: 04 July 2015
Accepted after revision: 31 August 2015
Publication Date:
21 October 2015 (online)
Abstract
Efficient strategies for the regioselective ortho acetoxylation/alkoxylation of C–H bond of azoxybenzenes in the presence of palladium catalysts were developed using PhI(OAc)2 as the teminal oxidant. Under the very similar conditions established, both reactions proceeded smoothly and were tolerated by a variety of functional groups.
Key words
palladium-catalyzed - acetoxylation–alkoxylation - C–H bond cleavage - azoxybenzene - regioselectiveSupporting Information
- Supporting information for this article is available online at http://dx.doi.org/10.1055/s-0035-1560637.
- Supporting Information
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