Synlett 2021; 32(18): 1784-1795
DOI: 10.1055/s-0040-1706031
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Suzuki–Miyaura Coupling Reactions of Fluorohalobenzenes

Shoaib Iqbal
a   Institut für Chemie, Universität Rostock, Albert-Einstein-Str. 3a, 18059 Rostock, Germany   URL: http://www.langer.chemie.uni-rostock.de/
b   Leibniz-Institut für Katalyse an der Universität Rostock e. V., Albert-Einstein-Str. 29a, 18059 Rostock, Germany
c   Department of Chemistry, COMSATS Institute of Information Technology, 22060, Abbottabad, Pakistan
,
Muhammad Sharif
a   Institut für Chemie, Universität Rostock, Albert-Einstein-Str. 3a, 18059 Rostock, Germany   URL: http://www.langer.chemie.uni-rostock.de/
b   Leibniz-Institut für Katalyse an der Universität Rostock e. V., Albert-Einstein-Str. 29a, 18059 Rostock, Germany
,
Peter Langer
a   Institut für Chemie, Universität Rostock, Albert-Einstein-Str. 3a, 18059 Rostock, Germany   URL: http://www.langer.chemie.uni-rostock.de/
b   Leibniz-Institut für Katalyse an der Universität Rostock e. V., Albert-Einstein-Str. 29a, 18059 Rostock, Germany
› Author Affiliations


Dedicated to Professor Ralf Miethchen on the occasion of his 80th birthday

Abstract

Organofluorine compounds have gained interest in the fields of pharmaceuticals, agrochemicals, diagnostics, materials, and catalysis. Suzuki–Miyaura coupling reactions of fluorinated arenes made a tremendous impact in chemical and biological research and made organofluorinated molecules more readily available. This review gives a brief summary of Suzuki–Miyaura coupling reactions of fluorinated benzene derivatives. In this context, various aspects, such as regio­selectivity, efficiency, and applications, are discussed.

1 Introduction

2 Organofluorine Compounds

3 Suzuki–Miyaura Reactions of Fluorohalobenzenes

3.1 Fluorophthalates

3.2 Reactions of Pentafluorohalobenzenes

3.3 Tetrafluorohalobenzenes

3.4 Trifluorohalobenzenes

3.5 Difluorohalobenzenes

3.6 Monofluorohalobenzenes

3.7 Halo(trifluoromethyl)benzenes

3.8 Trifluoromethyl Pyridines

4 S Summary



Publication History

Received: 17 February 2021

Accepted after revision: 27 February 2021

Article published online:
01 April 2021

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