Issue 24, 2001

Intermolecular hydroacylation of acrylate esters: a new route to 1,4-dicarbonylsElectronic supplementary information (ESI) available: experimental details. See http://www.rsc.org/suppdata/cc/b1/b107852f/

Abstract

1,4-Dicarbonyl compounds can be prepared using a Rh(I) mediated hydroacylation reaction between (2-aminopicolyl)imines and acrylate esters followed by acid hydrolysis.

Supplementary files

Article information

Article type
Communication
Submitted
31 Aug 2001
Accepted
15 Oct 2001
First published
22 Nov 2001

Chem. Commun., 2001, 2558-2559

Intermolecular hydroacylation of acrylate esters: a new route to 1,4-dicarbonyls

M. C. Willis and S. Sapmaz, Chem. Commun., 2001, 2558 DOI: 10.1039/B107852F

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