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Updated: Jun 9, 2026

Preparation of a Corannulene-functionalized Hexahelicene by Copper(I)-catalyzed Alkyne-azide Cycloaddition of Nonplanar Polyaromatic Units
Published on: September 18, 2016
Facile iterative synthesis of biphenyl dendrons with a functionalized focus
Ellen J Wren1, Xin Wang, Anthony Farlow
1Centre for Organic Photonics & Electronics, The University of Queensland, School of Chemistry & Molecular Biosciences, Chemistry Building, Queensland, Australia, 4072.
Abstract:
An iterative procedure gives 1,3,5-phenyl-linked dendrons of up to the fourth generation and enables the formation of different generations of iridium(III) complex-cored dendrimers. The convergent synthesis uses N,N'-1,8-naphthyl-3,5-dibromophenylboronamide as the key building block. The iterative synthesis cycle involves deprotection of the boronamide-focused dendron to form a boronic acid and subsequent Suzuki coupling either with the N,N'-1,8-naphthyl-3,5-dibromophenylboronamide to give the next dendron generation or with an activated core to form a dendrimer.
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