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Issue 21, 2006
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Base-catalysed asymmetric hydroamination/cyclisation of aminoalkenes utilising a dimeric chiral diamidobinaphthyl dilithium salt

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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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Publication details

The article was received on 03 Jan 2006, accepted on 28 Mar 2006 and first published on 11 Apr 2006


Article type: Communication
DOI: 10.1039/B518360J
Citation: Chem. Commun., 2006,0, 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, 0, 2221
    DOI: 10.1039/B518360J

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