| Literature DB >> 33645878 |
Peter Ribar1, Leoš Valenta2, Tomáš Šolomek1,3,4, Michal Juríček2,3.
Abstract
Nucleophilic addition of carbon-centered nucleophiles to nanographene ketones represents a valuable late-stage method for the functionalization of zigzag nanographenes, but its use is rare in the chemical literature. Using two model systems, non-Kekulé triangulene-4,8-dione and Kekulé anthanthrone, we identify unexpected regioselectivities and uncover the rules that govern these reactions. Considering the large number of nanographene ketones that have been reported since the pioneering work of Eric Clar, this method enables synthesis and exploration of hitherto unknown functionalized nanographenes.Entities:
Keywords: Fukui function analysis; Michael addition; nucleophilic addition; regioselectivity; zigzag nanographene
Year: 2021 PMID: 33645878 DOI: 10.1002/anie.202016437
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336