Heteroaromatic Tosylates in the Regioselective Heck Reaction

Chapter
Part of the Springer Theses book series (Springer Theses)

Abstract

Regioselective Heck reactions of electron rich olefins are as stated above traditionally conducted using aryl triflates as electrophiles. The formation of the crucial cationic palladium(II) complex is readily formed after the oxidative addition due to the weak coordinating abilities of the triflate anion. The employment of other sulfonate derivatives such as aryl tosylates in the Heck reaction, representing a more stable and less costly alternative to the aryl triflates, has hardly been described in the literature.

Keywords

Heck Reaction Triflate Anion Vinyl Amide Butyl Vinyl Butyl Vinyl Ether 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Springer-Verlag Berlin Heidelberg 2012

Authors and Affiliations

  1. 1.Department of Chemistry Aarhus UniversityAarhus CDenmark

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