Issue 90, 2014

Highly efficient synthesis and antioxidant capacity of N-substituted benzisoselenazol-3(2H)-ones

Abstract

A new, general one step synthesis of N-substituted benzisoselenazol-3(2H)-ones based on the reaction of o-iodobenzamides with lithium diselenide, is described. A series of alkyl and aryl derivatives was obtained in high yields (up to 98%). Their GPx-like antioxidant activity, tested by NMR, showed a significantly higher activity than ebselen.

Graphical abstract: Highly efficient synthesis and antioxidant capacity of N-substituted benzisoselenazol-3(2H)-ones

Supplementary files

Article information

Article type
Communication
Submitted
13 Aug 2014
Accepted
29 Sep 2014
First published
29 Sep 2014

RSC Adv., 2014,4, 48959-48962

Highly efficient synthesis and antioxidant capacity of N-substituted benzisoselenazol-3(2H)-ones

A. J. Pacuła, J. Ścianowski and K. B. Aleksandrzak, RSC Adv., 2014, 4, 48959 DOI: 10.1039/C4RA08631G

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements