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Issue 7, 2019
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Hydroaminoalkylation of sterically hindered alkenes with N,N-dimethyl anilines using a scandium catalyst

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Abstract

An atom- and step-economical C(sp3)–H addition of N,N-dimethyl anilines to various sterically demanding 1,1- and 1,2-disubstituted alkenes has been achieved by using a simple β-diketiminato ligand supported scandium dialkyl complex in combination with a borate compound. The corresponding C(sp3)–C(sp3) bond forming reaction occurs with excellent regioselectivities to give a variety of tertiary aromatic amines.

Graphical abstract: Hydroaminoalkylation of sterically hindered alkenes with N,N-dimethyl anilines using a scandium catalyst

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Supplementary files

Article information


Submitted
26 Oct 2018
Accepted
10 Dec 2018
First published
10 Dec 2018

Org. Biomol. Chem., 2019,17, 2013-2019
Article type
Paper

Hydroaminoalkylation of sterically hindered alkenes with N,N-dimethyl anilines using a scandium catalyst

J. Su, Y. Zhou and X. Xu, Org. Biomol. Chem., 2019, 17, 2013
DOI: 10.1039/C8OB02657B

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