Issue 34, 2008

Asymmetric intermolecular Stetter reactions catalyzed by a novel triazolium derived N-heterocyclic carbene

Abstract

The asymmetric intermolecular Stetter reaction is catalyzed by a novel triazolium salt derived N-heterocyclic carbene leading to 1,4-diketones in moderate to excellent yields (49–98%) and moderate to good enantioselectivities (56–78% ee), which could be enhanced by one recrystallization to excellent levels (90–99% ee).

Graphical abstract: Asymmetric intermolecular Stetter reactions catalyzed by a novel triazolium derived N-heterocyclic carbene

Supplementary files

Article information

Article type
Communication
Submitted
11 Jun 2008
Accepted
02 Jul 2008
First published
25 Jul 2008

Chem. Commun., 2008, 3989-3991

Asymmetric intermolecular Stetter reactions catalyzed by a novel triazolium derived N-heterocyclic carbene

D. Enders, J. Han and A. Henseler, Chem. Commun., 2008, 3989 DOI: 10.1039/B809913H

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