Issue 21, 2006
From the journal:

Chemical Communications

Base-catalysed asymmetric hydroamination/cyclisation of aminoalkenes utilising a dimeric chiral diamidobinaphthyl dilithium salt†

Patricia Horrillo Martínez,a   Kai C. Hultzsch*a  and  Frank Hampela  

* Corresponding authors

a Institut für Organische Chemie, Friedrich-Alexander Universität Erlangen-Nürnberg, Henkestr. 42, Erlangen, Germany
E-mail: hultzsch@chemie.uni-erlangen.de
Fax: +49-9131-8526865
Tel: +49-9131-8526866

Abstract

A dimeric proline derived diamidobinaphthyl dilithium salt represents the first example of a chiral main group metal based catalyst for asymmetric hydroamination/cyclisation reactions of aminoalkenes.

Graphical abstract: Base-catalysed asymmetric hydroamination/cyclisation of aminoalkenes utilising a dimeric chiral diamidobinaphthyl dilithium salt

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Article information

DOI
https://doi.org/10.1039/B518360J
Article type
Communication
Submitted
03 Jan 2006
Accepted
28 Mar 2006
First published
11 Apr 2006

Chem. Commun., 2006, 2221-2223

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Base-catalysed asymmetric hydroamination/cyclisation of aminoalkenes utilising a dimeric chiral diamidobinaphthyl dilithium salt

P. H. Martínez, K. C. Hultzsch and F. Hampel, Chem. Commun., 2006, 2221 DOI: 10.1039/B518360J

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