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Updated: Jan 18, 2026

Preparation of a Corannulene-functionalized Hexahelicene by CopperI-catalyzed Alkyne-azide Cycloaddition of Nonplanar Polyaromatic Units
Published on: September 18, 2016
Organosilicon Precursors for Efficient Aromatic Copper-Mediated Radiocyanation
Jay S Wright1, Richard Ma1, Casey J McCarthy1
1Department of Radiology, University of Michigan, Ann Arbor, MI, 48109, USA.
None:
Copper-mediated radiolabelling has transformed how (hetero)aromatic imaging agents are prepared for positron emission tomography (PET). However, current methods maintain critical stability, reactivity, and toxicity concerns paramount for safely and reproducibly generating radiomedicines. To overcome these limitations, a copper-mediated 11C-cyanation reaction is presented that leverages heptamethyltrisiloxanes as (hetero)aryl nucleophiles. Rapid ipso-radiocyanation occurs in conversions surpassing related precursors, while offering stability and safety advantages. Multiple bioactive scaffolds relevant to (pre)clinical PET were labelled to showcase the broader significance of this protocol. Most notably, an automated radiosynthesis of a κ-opioid receptor antagonist currently used in clinical PET studies is reported using this method. Overall, adopting aryl silane precursors will improve radiochemical space and support the production of PET nuclear medicines.
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