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Updated: Aug 28, 2026

Preparation of a Corannulene-functionalized Hexahelicene by Copper(I)-catalyzed Alkyne-azide Cycloaddition of Nonplanar Polyaromatic Units
Published on: September 18, 2016
C─S Bond Formation of Aryl Germanes
Jaime Ponce-de-León1, Markus D Schoetz1, Amit Dahiya1
1Institute of Organic Chemistry, RWTH Aachen University, Aachen, Germany.
Abstract:
Aryl germanes have emerged as robust and orthogonal coupling partners, but the chemistry enabling their functionalization is still in its infancy. Herein, we report the first C─S bond formation of aryl germanes. In contrast to conventional C─S cross-couplings of prefunctionalized arenes that largely rely on transition-metal catalysis, this transformation proceeds in the absence of a metal catalyst at room temperature and tolerates air and moisture. The reaction is orthogonal to common coupling handles, including aryl halides and aryl silanes, enabling selective thiolations in multifunctional molecules. Mechanistic studies support a radical-based aromatic substitution pathway.
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