Volume 38, Issue 23 pp. 3528-3530
Communication

The First Cyclodiasteromeric [3]Rotaxane

Roland Schmieder

Roland Schmieder

Kekulé-Institut für Organische Chemie und Biochemie der Universität, Gerhard-Domagk-Strasse 1, D-53121 Bonn, Germany, Fax: (+49) 228-735-662

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Gosia Hübner

Gosia Hübner

Kekulé-Institut für Organische Chemie und Biochemie der Universität, Gerhard-Domagk-Strasse 1, D-53121 Bonn, Germany, Fax: (+49) 228-735-662

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Christian Seel

Christian Seel

Kekulé-Institut für Organische Chemie und Biochemie der Universität, Gerhard-Domagk-Strasse 1, D-53121 Bonn, Germany, Fax: (+49) 228-735-662

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Fritz Vögtle

Fritz Vögtle

Kekulé-Institut für Organische Chemie und Biochemie der Universität, Gerhard-Domagk-Strasse 1, D-53121 Bonn, Germany, Fax: (+49) 228-735-662

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Abstract

A mechanically linked molecule, consisting of an axle and two equivalent wheels, shows an analogous stereochemistry to the classical example tartaric acid. Though the components are not chiral themselves, a (cyclo)diastereomeric species is obtained, the enantiomers (shown schematically) and the meso form of which were completely separated and chiroptically characterized.

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