Frontispiece: Polyaniline‐Induced Arylation with Arenediazonium Salts Derived from Anilines
Dai Hata, Toshiyuki Moriuchi, Toshikazu Hirao, Toru Amaya
Abstract
Open-access reader
Dai Hata, Toshiyuki Moriuchi, Toshikazu Hirao, Toru Amaya
Abstract
Open-access reader
Polyaniline-induced C−H arylation of arenes with arenediazonium salts prepared by diazotization of anilines has been developed, whereby the amino group on the aniline is a formal leaving group. This sequential reaction proceeds in the presence of a catalytic amount of the reduced form of polyaniline under mild conditions without any metals or strong bases at room temperature to yield biaryls. More information can be found in the Full Paper by T. Amaya et al. on page 7703 ff.
OpenAlex reports 1 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Polyaniline-induced C−H arylation of arenes with arenediazonium salts prepared by diazotization of anilines has been developed, whereby the amino group on the aniline is a formal leaving group. This sequential reaction proceeds in the presence of a catalytic amount of the reduced form of polyaniline under mild conditions without any metals or strong bases at room temperature to yield biaryls. More information can be found in the Full Paper by T. Amaya et al. on page 7703 ff.
Key concepts: Polyaniline, Aniline, Yield (engineering), Catalysis, Chemistry, Group (periodic table), Polymer chemistry, Reaction conditions