Issue 49, 2014

Iron-catalysed tandem isomerisation/hydrosilylation reaction of allylic alcohols with amines

Abstract

An iron(0)-catalysed cascade synthesis of N-alkylated anilines from allylic or homoallylic alcohols and primary and secondary anilines under hydrosilylation conditions has been developed. Notably, a simple Fe(cod)(CO)3 complex (cod = cycloocta-1,5-diene) was used as a precatalyst under visible light activation in ethanol in the presence of the inexpensive and non-toxic PMHS (polymethylhydrosiloxane) as the hydrosilane source. This methodology is based on a three step-one sequence process involving isomerisation of allylic alcohols/condensation with anilines/reduction reactions.

Graphical abstract: Iron-catalysed tandem isomerisation/hydrosilylation reaction of allylic alcohols with amines

Supplementary files

Article information

Article type
Communication
Submitted
21 Feb 2014
Accepted
29 May 2014
First published
29 May 2014

RSC Adv., 2014,4, 25892-25897

Iron-catalysed tandem isomerisation/hydrosilylation reaction of allylic alcohols with amines

H. Li, M. Achard, C. Bruneau, J. Sortais and C. Darcel, RSC Adv., 2014, 4, 25892 DOI: 10.1039/C4RA04037F

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