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Direct arylation and heterogeneous catalysis; ever the twain…
Chemical
Science
PERSPECTIVE View Article Online
View Journal | View Issue
. Direct arylation and heterogeneous catalysis; ever
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c
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e the twain shall meet
c
i
L Cite this: Chem. Sci., 2015, 6, 5338
5. d ab c ab
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5 r Rafael Cano, Alexander F. Schmidt* and Gerard P. McGlacken*
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4
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1 The formation of aryl –aryl bonds and heteroaryl analogues is one of the most important C–C bond forming
6 0.
1 3 processes in organic chemistry. Recently, a methodology termed Direct Arylation (DA) has emerged as an
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2 n
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1 i attractive alternative to traditional cross-coupling reactions (Suzuki–Miyaura, Stille, Negishi, etc.). A parallel
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3 i focus of the pharmaceutical and other chemical industries has been on the use heterogeneous catalysis as a
1 r
t
n t
o A favourable substitute for its homogeneous counterpart in cross-coupling reactions. Only very recently has
d s
e n heterogeneous catalysis been proposed and applied, to DA reactions. In this perspective, we consider the
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