Issue 3, 1978

Radical alkyldenitration. A synthetically useful example of homolytic aromatic Ipso-substitution reactions

Abstract

Nucleophilic alkyl radicals react with nitroaromatic compounds to give alkyldenitration products in good yields; in benzene derivatives displacement of the nitro-group occurs easily when an electron-withdrawing substituent is present in the para position.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1978, 93-94

Radical alkyldenitration. A synthetically useful example of homolytic aromatic Ipso-substitution reactions

L. Testaferri, M. Tiecco, M. Tingoli, M. Fiorentino and L. Troisi, J. Chem. Soc., Chem. Commun., 1978, 93 DOI: 10.1039/C39780000093

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.

Spotlight

Advertisements