Issue 17, 2001

Powerful Claisen condensation and Claisen–aldol tandem reaction of α,α-dialkylated esters promoted by ZrCl4iPr2NEt

Abstract

Powerful Claisen ester condensations of α,α-dialkylated esters mediated by ZrCl4iPr2NEt were performed to give the corresponding thermodynamically unfavorable α,α-dialkylated β-ketoesters, and Claisen–aldol tandem reactions between an intermediary Zr-enolate of a α,α-dialkylated β-ketoester and aldehydes also proceeded.

Graphical abstract: Powerful Claisen condensation and Claisen–aldol tandem reaction of α,α-dialkylated esters promoted by ZrCl4–iPr2NEt

Article information

Article type
Communication
Submitted
14 May 2001
Accepted
19 Jul 2001
First published
07 Aug 2001

Chem. Commun., 2001, 1674-1675

Powerful Claisen condensation and Claisen–aldol tandem reaction of α,α-dialkylated esters promoted by ZrCl4iPr2NEt

Y. Tanabe, R. Hamasaki and S. Funakoshi, Chem. Commun., 2001, 1674 DOI: 10.1039/B104185C

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