Issue 9, 2024

An iron-catalyzed nitrene transfer reaction of nitrosobenzenes with N-acyloxyamides for accessing N-acyl azoxy molecules

Abstract

Reported herein is a nitrene transfer reaction of nitrosobenzenes with N-acyloxyamides using FeCl2ยท4H2O as a cheap and commercially available catalyst, affording N-acyl azoxy compounds with high functional-group compatibility. This facile transformation could be carried out smoothly under an air atmosphere at the gram scale and its synthetic utility was demonstrated by efficient reduction and aryl transfer reactions of the product.

Graphical abstract: An iron-catalyzed nitrene transfer reaction of nitrosobenzenes with N-acyloxyamides for accessing N-acyl azoxy molecules

Supplementary files

Article information

Article type
Research Article
Submitted
22 Jan 2024
Accepted
03 Mar 2024
First published
06 Mar 2024

Org. Chem. Front., 2024,11, 2561-2565

An iron-catalyzed nitrene transfer reaction of nitrosobenzenes with N-acyloxyamides for accessing N-acyl azoxy molecules

W. Huang, H. Yan, Q. Wang, J. Chen, Y. Luo and Y. Xia, Org. Chem. Front., 2024, 11, 2561 DOI: 10.1039/D4QO00137K

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