Abteilung Chemische Biologie, Max-Planck-Institut für Molekulare Physiologie, Otto-Hahn-Strasse 11, 44227 Dortmund (Germany); Fakultät Chemie und Chemische Biologie, Technische Universität Dortmund, Otto-Hahn-Strasse 6, 44221 Dortmund (Germany).
Angew Chem Int Ed Engl. 2014 Jul 28;53(31):8163-6. doi: 10.1002/anie.201403712. Epub 2014 Jun 18.
A novel annulation reaction between 2-aminopyridine derivatives and arenes under metal-free conditions is described. The presented intermolecular transformation provided straightforward access to the important pyrido[1,2-a]benzimidazole scaffold under mild reaction conditions. The unprecedented application of the methyl group of methylbenzenes as a traceless, non-chelating, and highly regioselective directing group is reported.
描述了一种在无金属条件下 2-氨基吡啶衍生物和芳烃之间的新型环化反应。所提出的分子间转化在温和的反应条件下为重要的吡啶并[1,2-a]苯并咪唑支架提供了直接的途径。报告了甲基苯的甲基作为无痕迹、非螯合和高区域选择性导向基团的前所未有的应用。