Issue 5, 2013
From the journal:

Catalysis Science & Technology

Regioselective Pd-catalyzed hydroamination of substituted dienes

Arnaud Perrier,a   Michel Ferreira,†a   Joost N. H. Reeka  and  Jarl Ivar van der Vlugt*a  

* Corresponding authors

a Homogeneous & Supramolecular Catalysis, van't Hoff Institute for Molecular Sciences, University of Amsterdam, Science Park 904, Amsterdam, The Netherlands
E-mail: j.i.vandervlugt@uva.nl
Fax: +31 (0)20 525 5604
Tel: +31 (0)20 525 6459

Abstract

The regioselective addition of hydrazones and related N-nucleophiles to substituted terpene-based substrates can be steered to either 1,2- or 1,4-addition products, making this a potentially powerful protocol for the preparation of amines from biorelevant feedstocks via C–N bond formation.

Graphical abstract: Regioselective Pd-catalyzed hydroamination of substituted dienes

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/C3CY00024A
Article type
Paper
Submitted
09 Jan 2013
Accepted
18 Feb 2013
First published
19 Feb 2013
This article is Open Access

Catal. Sci. Technol., 2013,3, 1375-1379

Permissions

Request permissions

Regioselective Pd-catalyzed hydroamination of substituted dienes

A. Perrier, M. Ferreira, J. N. H. Reek and J. I. van der Vlugt, Catal. Sci. Technol., 2013, 3, 1375 DOI: 10.1039/C3CY00024A

This is an Open Access article. The full version of this article can be posted on a website/blog, posted on an intranet, photocopied, emailed, distributed in a course pack or distributed in Continuing Medical Education (CME) materials provided that it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, 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 commercial 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