Issue 17, 2010

Recent advances in transition metal-catalyzed N-atom transfer reactions of azides

Abstract

Transition metal-catalyzed N-atom transfer reactions of azides provide efficient ways to construct new carbonnitrogen and sulfurnitrogen bonds. These reactions are inherently green: no additive besides catalyst is needed to form the nitrenoid reactive intermediate, and the by-product of the reaction is environmentally benign N2 gas. As such, azides can be useful precursors for transition metal-catalyzed N-atom transfer to sulfides, olefins and C–H bonds. These methods offer competitive selectivities and comparable substrate scope as alternative processes to generate metal nitrenoids.

Graphical abstract: Recent advances in transition metal-catalyzed N-atom transfer reactions of azides

Article information

Article type
Perspective
Submitted
22 Apr 2010
First published
08 Jul 2010

Org. Biomol. Chem., 2010,8, 3831-3846

Recent advances in transition metal-catalyzed N-atom transfer reactions of azides

T. G. Driver, Org. Biomol. Chem., 2010, 8, 3831 DOI: 10.1039/C005219C

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