M-lodosylbenzoic acid - A convenient recyclable reagent for highly efficient aromatic iodinations

21Citations
Citations of this article
17Readers
Mendeley users who have this article in their library.

Abstract

m-lodosylbenzoic acid performs iodinations of arenes in the presence of iodine at room temperature in acetonitrile. Separation of pure products is conveniently achieved by scavenging any aryl iodide by ion exchange with IRA-900 (hydroxide form). The reduced form of the reagent, m-iodobenzoic acid, can be easily recovered from the ion exchange resin or from the basic aqueous solution by simple acidification with HCl.

Cite

CITATION STYLE

APA

Kirschning, A., Yusubov, M. S., Yusubova, R. Y., Chi, K. W., & Park, J. Y. (2007). M-lodosylbenzoic acid - A convenient recyclable reagent for highly efficient aromatic iodinations. Beilstein Journal of Organic Chemistry, 3. https://doi.org/10.1186/1860-5397-3-19

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free