Mizoroki–Heck Reactions with 4??Phenoldiazonium Salts

B Schmidt, F Hölter, R Berger…

Index: Schmidt, Bernd; Hoelter, Frank; Berger, Rene; Jessel, Soenke Advanced Synthesis and Catalysis, 2010 , vol. 352, # 14-15 p. 2463 - 2473

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Citation Number: 39

Abstract

Abstract Significantly better yields were achieved in Mizoroki–Heck reactions using 4- phenoldiazonium salts instead of their O-alkylated analogues under otherwise identical conditions. We found that a one-flask deacetylation–diazotation–precipitation sequence starting from paracetamol or acetanilides derived thereof provides a convenient access to the required diazonium tetrafluoroborates. The utility of these arylating agents in ...

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