© WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Editor: Michael Rowan; Editorial Board Chairs: Uwe Bornscheuer, Luis A. Oro, Bert Weckhuysen
Impact Factor: 4.724
ISI Journal Citation Reports © Ranking: 2015: 29/144 (Chemistry Physical)
Online ISSN: 1867-3899
Cover Picture: A Theoretical Study of the Mechanism of the Desymmetrization of Cyclic meso-Anhydrides by Chiral Amino Alcohols (ChemCatChem 9/2010)
The cover picture shows the reaction coordinate for the alcoholysis of cyclic meso-anhydrides catalyzed by α-amino alcohols. Starting from the left, the reaction has two pathways, either general base catalysis (blue) or nucleophilic catalysis (orange). In their article on pages 1122–1129, Aviyente and co-workers identify the transition structures along the general base and the nucleophilic catalysis pathways. The energy required to pass through the barrier in the general base catalysis pathway is less than that required in the nucleophilic catalysis pathway.