Issue 72, 2014

An organocatalytic cascade reaction of 2-nitrocyclohexanone and α,β-unsaturated aldehydes with unusual regioselectivity

Abstract

An organocatalytic cascade reaction of 2-nitrocyclohexanone and α,β-unsaturated aldehydes was developed. Bicyclo[3.3.1]nonanone products were obtained with good yields and excellent enantioselectivities. The reaction occurred with unusual regioselectivity. A dienolate-iminium activation mechanism was proposed. The products were transformed to eight-membered cyclic ketones with high enantioselectivity.

Graphical abstract: An organocatalytic cascade reaction of 2-nitrocyclohexanone and α,β-unsaturated aldehydes with unusual regioselectivity

Supplementary files

Article information

Article type
Communication
Submitted
05 Jun 2014
Accepted
22 Jul 2014
First published
22 Jul 2014

Chem. Commun., 2014,50, 10471-10473

Author version available

An organocatalytic cascade reaction of 2-nitrocyclohexanone and α,β-unsaturated aldehydes with unusual regioselectivity

Y. Xuan, Z. Chen and M. Yan, Chem. Commun., 2014, 50, 10471 DOI: 10.1039/C4CC04298K

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