Issue 36, 2015

Palladium-catalyzed oxygenation of C(sp2)–H and C(sp3)–H bonds under the assistance of oxalyl amide

Abstract

A practical palladium-catalyzed γ-oxygenation of C(sp2)–H and C(sp3)–H bonds under the assistance of oxalyl amide with PhI(OAc)2 as oxidant was developed. Selective alkoxylation or acetoxylation of oxalyl amide protected benzyl amine was achieved in high yield. The oxalyl amide protected α-substituted propylamines could be transformed into acetoxylated products in good to excellent yields.

Graphical abstract: Palladium-catalyzed oxygenation of C(sp2)–H and C(sp3)–H bonds under the assistance of oxalyl amide

Supplementary files

Article information

Article type
Communication
Submitted
09 Jan 2015
Accepted
17 Mar 2015
First published
17 Mar 2015

RSC Adv., 2015,5, 28430-28434

Author version available

Palladium-catalyzed oxygenation of C(sp2)–H and C(sp3)–H bonds under the assistance of oxalyl amide

P. Liu, J. Han, C. P. Chen, D. Q. Shi and Y. S. Zhao, RSC Adv., 2015, 5, 28430 DOI: 10.1039/C5RA00114E

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