Issue 19, 2020

Diamine-mediated degradative dimerisation of Morita–Baylis–Hillman ketones

Abstract

A degradative dimerisation of Morita–Baylis–Hillman ketones was observed in the presence of a primary diamine. The reaction proceeded swiftly to produce methylene-bridged 1,3-dicarbonyl compounds. A brief mechanistic investigation alluded to a retro-Mannich reaction as the key step of the transformation.

Graphical abstract: Diamine-mediated degradative dimerisation of Morita–Baylis–Hillman ketones

Supplementary files

Article information

Article type
Communication
Submitted
30 Dec 2019
Accepted
03 Feb 2020
First published
03 Feb 2020

Chem. Commun., 2020,56, 2949-2952

Diamine-mediated degradative dimerisation of Morita–Baylis–Hillman ketones

A. K. Jha, A. Kumari and S. Easwar, Chem. Commun., 2020, 56, 2949 DOI: 10.1039/C9CC10068G

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