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Updated: Feb 20, 2026

Preparation of a Corannulene-functionalized Hexahelicene by CopperI-catalyzed Alkyne-azide Cycloaddition of Nonplanar Polyaromatic Units
Published on: September 18, 2016
C3 -Symmetric Tricyclo[2.2.1.02,6 ]heptane-3,5,7-triol
Volodymyr Kozel1, Constantin-Gabriel Daniliuc1, Peer Kirsch2
1Organisch-Chemisches Institut, Universität Münster, Corrensstrasse 40, 48149, Münster, Germany.
Abstract:
A straightforward access to a hitherto unknown C3 -symmetric tricyclic triol both in racemic and enantiopure forms has been developed. Treatment of 7-tert-butoxynorbornadiene with peroxycarboxylic acids provided mixtures of C1 - and C3 -symmetric 3,5,7-triacyloxynortricyclenes via transannular π-cyclization and replacement of the tert-butoxy group. By refluxing in formic acid, the C1 -symmetric esters were converted to the C3 -symmetric formate. Hydrolysis gave diastereoisomeric triols, which were separated by recrystallization. Enantiomer resolution via diastereoisomeric tri(O-methylmandelates) delivered the target triols on a gram scale. The pure enantiomers are useful as core units of dopants for liquid crystals.
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