4.4 Article

Palladium-catalyzed acetoxylation of arenes by 1,2,3-triazole-directed C-H activation

Journal

TETRAHEDRON LETTERS
Volume 58, Issue 7, Pages 614-617

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2016.12.086

Keywords

Palladium; C-H activation; 1,4-Disubstituted-1,2,3-triazoles; Acetoxylation; Regioselectivity

Funding

  1. National Natural Science Foundation of China [21662020, 51363012]

Ask authors/readers for more resources

A facile and efficient method for the regioselective acetoxylation of 1,4-disubstituted 1,2,3-triazoles via Pd-catalyzed C-H bond activation was developed. The cheap acetic acid was applied as the acetoxyl source to convert aromatic sp(2) C-H bonds into C-O bonds in high regioselectivity, employing 1,2,3-triazole as an elegant directing group and K2S2O8 as the oxidant. A range of 1,2,3-triazoles bearing acetoxyl group can be synthesized with the reaction facilely. (C) 2017 Elsevier Ltd. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.4
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available