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Inside Back Cover: A Brønsted Acid Catalyzed Redox Arylation (Angew. Chem. Int. Ed. 33/2014)
Author(s) -
Peng Bo,
Huang Xueliang,
Xie LanGui,
Maulide Nuno
Publication year - 2014
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Reports
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.201406163
Subject(s) - catalysis , redox , int , cover (algebra) , joins , reagent , chemistry , aryl , proton , brønsted–lowry acid–base theory , work (physics) , physics , organic chemistry , computer science , engineering , thermodynamics , mechanical engineering , nuclear physics , operating system , alkyl , programming language
The catalytic redox‐neutral arylation of ynamides with aryl sulfoxides is described by N. Maulide et al. in their Communication on page 8718 ff. This reaction is illustrated by the harmonious catalysis of a proton that joins the two reagents in an atom‐economic manner. The background depicts the harmonious collaboration between the two institutions where this work was carried out: the Max‐Planck‐Institut für Kohlenforschung and the University of Vienna.