Issue 75, 2019

Dioxazolones as masked ester surrogates in the Pd(ii)-catalyzed direct C–H arylation of 6,5-fused heterocycles

Abstract

A simple and effective Pd(II)-catalyzed regioselective C(2)–H arylation of 6,5-fused heterocycles with dioxazolones as a masked ester surrogate under mild conditions is reported. The significance of the arylation is highlighted by the new reactivity demonstrated in dioxazolones via proximal C–H activation of the cyclic carbonate of the hydroxamic acid functionality under protic conditions.

Graphical abstract: Dioxazolones as masked ester surrogates in the Pd(ii)-catalyzed direct C–H arylation of 6,5-fused heterocycles

Supplementary files

Article information

Article type
Communication
Submitted
18 Jul 2019
Accepted
19 Aug 2019
First published
20 Aug 2019

Chem. Commun., 2019,55, 11187-11190

Dioxazolones as masked ester surrogates in the Pd(II)-catalyzed direct C–H arylation of 6,5-fused heterocycles

P. Saxena, N. Maida and M. Kapur, Chem. Commun., 2019, 55, 11187 DOI: 10.1039/C9CC05563K

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