Issue 36, 2017

Kinetic resolution via supramolecular iminium catalysis: multiactivation enables the asymmetric synthesis of β-aryl substituted aldehydes and densely functionalized cyclohexanes

Abstract

The kinetic resolution of β-aryl substituted 1,7-dioxo compounds with α,β-unsaturated aldehydes affording enantioenriched β-aryl substituted aldehydes as well as densely functionalized cyclohexanes is presented. The two enantioenriched products were obtained in reasonable yields with high diastereo- and enantioselectivities under supramolecular iminium catalysis which activates both the substrates and the reactive intermediates.

Graphical abstract: Kinetic resolution via supramolecular iminium catalysis: multiactivation enables the asymmetric synthesis of β-aryl substituted aldehydes and densely functionalized cyclohexanes

Supplementary files

Article information

Article type
Communication
Submitted
02 Mar 2017
Accepted
31 Mar 2017
First published
31 Mar 2017

Chem. Commun., 2017,53, 4938-4941

Kinetic resolution via supramolecular iminium catalysis: multiactivation enables the asymmetric synthesis of β-aryl substituted aldehydes and densely functionalized cyclohexanes

Z. Jia, Y. Wang, G. Xu and P. Xu, Chem. Commun., 2017, 53, 4938 DOI: 10.1039/C7CC01625E

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