Volume 38, Issue 23 pp. 3474-3477
Communication

The First Enantiomerically Pure Triangulane (M)-Trispiro[2.0.0.2.1.1]nonane Is a σ-[4]Helicene

Armin de Meijere

Armin de Meijere

Institut für Organische Chemie der Universität, Tammannstrasse 2, D-37077 Göttingen, Germany, Fax: (+49) 551-39-9475

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Alexander F. Khlebnikov

Alexander F. Khlebnikov

St. Petersburg State University, Chemical Department, St.-Petersburg, Russia

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Rafael R. Kostikov

Rafael R. Kostikov

St. Petersburg State University, Chemical Department, St.-Petersburg, Russia

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Sergei I. Kozhushkov

Sergei I. Kozhushkov

Institut für Organische Chemie der Universität, Tammannstrasse 2, D-37077 Göttingen, Germany, Fax: (+49) 551-39-9475

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Peter R. Schreiner

Peter R. Schreiner

Institut für Organische Chemie der Universität, Tammannstrasse 2, D-37077 Göttingen, Germany, Fax: (+49) 551-39-9475

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Alexander Wittkopp

Alexander Wittkopp

Institut für Organische Chemie der Universität, Tammannstrasse 2, D-37077 Göttingen, Germany, Fax: (+49) 551-39-9475

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Dmitrii S. Yufit

Dmitrii S. Yufit

Department of Chemistry, University of Durham, Durham, UK

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Abstract

A remarkably high specific rotation, even at 589 nm, is shown by (M)-1, the first enantiomerically pure unbranched [4]triangulane, although it has no chromophore that would lead to any significant absorption above 200 nm. This outstanding rotatory power is in line with a helical arrangement of its σ bonds, as confirmed by high-level computations. Thus, it is appropriate to call (M)-1 a “σ-[4]helicene”, the first σ-bond analogue of the aromatic [n]helicenes.

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