Assembly of Biaryl Amines via Mild Copper-Catalyzed Coupling of Anilines with (Hetero)aryl Chlorides/Bromides
Sailuo Li,
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Lanting Xu,
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Bang An
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et al.
Organic Letters,
Journal Year:
2025,
Volume and Issue:
27(6), P. 1498 - 1503
Published: Jan. 31, 2025
CuI/6-hydroxy
picolinohydrazide-catalyzed
coupling
of
(hetero)aryl
chlorides
with
anilines
proceeded
well
at
100
°C
to
afford
biaryl
amines
in
a
diverse
manner,
which
represents
the
first
example
Cu-catalyzed
under
milder
conditions.
The
same
catalytic
system
could
make
bromides
work
room
temperature,
giving
corresponding
products
an
excellent
reaction
scope.
Language: Английский
Cu-Catalyzed Synthesis of Symmetric Diarylamines from Organoboronic Acids Using NaNO2 as the Amino Source
Daming Liu,
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Hui You,
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Shuo Zhang
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et al.
The Journal of Organic Chemistry,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 7, 2025
A
copper-catalyzed
novel
synthesis
of
symmetric
diarylamines
was
achieved
from
aryl
boronic
acids
and
NaNO2.
This
protocol
employs
as
the
commercially
available
arylation
reagents
sodium
nitrite
(NaNO2)
cheap,
stable,
solid
amino
source.
Under
a
simple
ligand-
base-free
copper
catalytic
system
(CuCl
sole
catalyst),
wide
range
could
be
obtained
in
moderate
to
good
yields.
Notably,
use
Na15NO2
produce
15N-labeled
diarylamines,
which
would
otherwise
difficult
prepare
by
known
methods.
Language: Английский