Issue 13, 2016

AlCl3-catalyzed [3 + 3] cycloaddition of chalcones and β-enamine ketones (esters): a highly efficient access to multisubstituted cyclohexa-1,3-dienamines

Abstract

AlCl3-catalyzed [3 + 3] intermolecular cycloaddition of enones with enamines is described. This efficient protocol was successfully achieved to give 1,3-cyclohexadiene derivatives in good to excellent yields.

Graphical abstract: AlCl3-catalyzed [3 + 3] cycloaddition of chalcones and β-enamine ketones (esters): a highly efficient access to multisubstituted cyclohexa-1,3-dienamines

Supplementary files

Article information

Article type
Paper
Submitted
02 Dec 2015
Accepted
15 Jan 2016
First published
19 Jan 2016

RSC Adv., 2016,6, 10943-10948

AlCl3-catalyzed [3 + 3] cycloaddition of chalcones and β-enamine ketones (esters): a highly efficient access to multisubstituted cyclohexa-1,3-dienamines

M. Xing, H. Xu, L. Hou, J. Gao and Y. Li, RSC Adv., 2016, 6, 10943 DOI: 10.1039/C5RA25691G

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