Issue 22, 2000

Amination of benzylic C–H bonds by aryl azides catalysed by CoII(porphyrin) complexes. A new reaction leading to secondary amines and iminesFormulae of the catalysts and of the organic products and Fig. 1, the influence of the toluene concentration on the value of kapp are available as supplementary data. For direct electronic access see http://www.rsc.org/suppdata/cc/b0/b006136k/

Abstract

CoII(porphyrin) complexes catalyse the reaction of aromatic azides, ArN3, with hydrocarbons containing a benzylic group, R1R2R3CH, to give the corresponding amines, R1R2R3C-NHAr. When at least one of the R1–R3 substituents is hydrogen, the catalytic reaction proceeds further to give the imines R1R2C[double bond, length half m-dash]NAr in good yields.

Supplementary files

Article information

Article type
Communication
Submitted
02 Aug 2000
Accepted
05 Oct 2000
First published
03 Nov 2000

Chem. Commun., 2000, 2265-2266

Amination of benzylic C–H bonds by aryl azides catalysed by CoII(porphyrin) complexes. A new reaction leading to secondary amines and imines

S. Cenini, E. Gallo, A. Penoni, F. Ragaini and S. Tollari, Chem. Commun., 2000, 2265 DOI: 10.1039/B006136K

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