Synthesis 2016; 48(11): 1597-1606
DOI: 10.1055/s-0035-1561586
short review
© Georg Thieme Verlag Stuttgart · New York

Recent Advances in Meerwein Arylation Chemistry

Authors

  • Stephanie Kindt

    Department of Chemistry and Pharmacy, Pharmaceutical Chemistry, Friedrich-Alexander-Universität Erlangen-Nürnberg, Schuhstraße 19, 91052 Erlangen, Germany   Email: Markus.Heinrich@fau.de
  • Markus R. Heinrich*

    Department of Chemistry and Pharmacy, Pharmaceutical Chemistry, Friedrich-Alexander-Universität Erlangen-Nürnberg, Schuhstraße 19, 91052 Erlangen, Germany   Email: Markus.Heinrich@fau.de
Further Information

Publication History

Received: 25 February 2016

Accepted after revision: 29 February 2016

Publication Date:
31 March 2016 (online)


Graphical Abstract

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Abstract

The Meerwein arylation has recently received much attention and a variety of new variants have been developed. Advances include new sources for aryl radicals, new radical scavengers, as well as improved reaction conditions. This short review summarizes important developments that make this radical-type reaction an even more powerful tool for the diverse functionalization of alkenes.

1 Introduction

2 Meerwein Arylations

2.1 Carboarylation

2.2 Carboamination

2.3 Carbooxygenation

2.4 Carbothiolation

2.5 Carbofluorination

3 Summary