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Ruthenium(II)-Catalyzed Double Annulation of Quinones: Step-Economical Access to Valuable Bioactive Compounds
Authors:Prof Dr Eufrânio N da Silva Júnior  Renato L de Carvalho  Renata G Almeida  Luisa G Rosa  Dr Felipe Fantuzzi  Dr Torben Rogge  Pedro M S Costa  Prof Dr Claudia Pessoa  Prof Dr Claus Jacob  Prof Dr Lutz Ackermann
Institution:1. Institut für Organische und Biomolekulare Chemie, Georg-August-Universität Göttingen, Tammannstraße 2, 37077 Göttingen, Germany;2. Institut für Organische und Biomolekulare Chemie, Georg-August-Universität Göttingen, Tammannstraße 2, 37077 Göttingen, Germany

Institute of Exact Sciences, Department of Chemistry, Federal University of Minas Gerais, UFMG, 31270-901 Belo Horizonte, MG, Brazil;3. Institute of Exact Sciences, Department of Chemistry, Federal University of Minas Gerais, UFMG, 31270-901 Belo Horizonte, MG, Brazil;4. Institute for Inorganic Chemistry, Julius-Maximilians-Universität Würzburg, Am Hubland, 97074 Würzburg, Germany;5. Department of Physiology and Pharmacology, Federal University of Ceará, Fortaleza, CE, 60430-270 Brazil;6. Division of Bioorganic Chemistry, School of Pharmacy, University of Saarland, 66123 Saarbrücken, Germany

Abstract:Double ruthenium(II)-catalyzed alkyne annulations of quinones were accomplished. Thus, a strategy is reported that provides step-economical access to valuable quinones with a wide range of applications. C−H/N−H activations for alkyne annulations of naphthoquinones provided challenging polycyclic quinoidal compounds by forming four new bonds in one step. The singular power of the thus-obtained compounds was reflected by their antileukemic activity.
Keywords:alkynes  annulation  C−H activation  quinones  ruthenium
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