Tuning the Catalyst Reactivity of Imidazolylidene Catalysts through Substituent Effects on the N‑Aryl Groups

A series of imidazolium salts with various N-aryl groups were synthesized, and their catalytic activities were evaluated to investigate the contribution of the N-aryl groups to the catalytic activity in the synthesis of γ-butyrolactone through an a3→d3-umpolung addition. Imidazolylidenes with 2,6-di...

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Veröffentlicht in:Organic letters 2017-05, Vol.19 (10), p.2750-2753
Hauptverfasser: Kyan, Ryuji, Sato, Kohei, Mase, Nobuyuki, Watanabe, Naoharu, Narumi, Tetsuo
Format: Artikel
Sprache:eng
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Zusammenfassung:A series of imidazolium salts with various N-aryl groups were synthesized, and their catalytic activities were evaluated to investigate the contribution of the N-aryl groups to the catalytic activity in the synthesis of γ-butyrolactone through an a3→d3-umpolung addition. Imidazolylidenes with 2,6-diethylphenyl groups were effective catalysts, and several mechanistic studies, including a deuterium kinetic isotope effect study, revealed that both steric and kinetic effects were responsible for the enhanced catalytic activity.
ISSN:1523-7060
1523-7052
DOI:10.1021/acs.orglett.7b01105