Mannitol‐based CO Surrogate for Palladium‐Catalyzed Alkoxycarbonylation
Z. W. Liu,
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Hefei Yang,
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Zhipeng Bao
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et al.
European Journal of Organic Chemistry,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 6, 2025
Abstract
Carbonylative
transformation
is
already
been
accepted
as
a
powerful
toolbox
in
synthetic
chemistry.
However,
the
manipulation
of
toxic
and
smell‐less
carbon
monoxide
gas
lagged
it
from
wide
range
applications.
Hence
developing
new
efficient
CO
surrogates
become
an
attractive
topic.
Herein,
we
developed
novel
mannitol‐based
surrogate
with
enhanced
loading
capacity
compared
to
known
organic
surrogates.
We
successfully
used
palladium‐catalyzed
alkoxycarbonylation
aryl
bromides
phenols
only
0.5
equivalent
required.
This
newly
designed
offers
additional
possibility
for
further
development
Language: Английский
Construction of Six-Membered Lactam and Lactone Structures via Ligand-Free Pd-Catalyzed C–H Activation/[5 + 1] Cyclization Carbonylation
Chengxian Hu,
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Lu Wang,
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Xue Yang
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et al.
Organic Letters,
Journal Year:
2024,
Volume and Issue:
26(37), P. 7783 - 7788
Published: Sept. 9, 2024
An
approach
for
the
ligand-free
Pd-catalyzed
C-H
activation/[5
+
1]
cyclization
carbonylation
by
employing
readily
available
ClCF
Language: Английский
Palladium-catalyzed difluorocarbene transfer enables access to enantioenriched chiral spirooxindoles
Zhiwen Nie,
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Keqin Wu,
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Xiaohang Zhan
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et al.
Nature Communications,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: Oct. 1, 2024
Language: Английский
Synthesis of 2-Fluorinated Pyrazolo[1,5-a]pyridines via Base- Mediated [3+2] Cycloaddition of N-Aminopyridinium Salts with gem-Difluorostyrenes
Yang Feng,
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Yuanyuan Wu,
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Zengjiang Yue
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et al.
New Journal of Chemistry,
Journal Year:
2024,
Volume and Issue:
48(28), P. 12496 - 12500
Published: Jan. 1, 2024
A
method
for
the
construction
of
2-fluoropyrazolo[1,5-
a
]pyridines
through
base-promoted
[3+2]
cycloaddition
N
-aminopyridinium
salts
with
gem
-difluorostyrenes
has
been
established.
Language: Английский
The [PdCl2(Xantphos)] Complex Efficiently Catalyzed the Methoxycarbonylation of Iodobenzene to Methyl Benzoate
Luca Pietrobon,
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Lucio Ronchin,
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Andrea Vavasori
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et al.
Catalysts,
Journal Year:
2024,
Volume and Issue:
14(10), P. 660 - 660
Published: Sept. 24, 2024
The
[PdCl2(Xantphos)]
complex,
in
comparison
with
several
[PdCl2(P–P)]
complexes
having
different
diphosphine
chelating
ligands
(P–P),
is
very
active
as
a
catalyst
for
the
carbonylation
of
iodobenzene
to
methyl
benzoate.
run
conditions
and
influence
cocatalysts
have
been
also
studied
further
improve
catalytic
activity.
optimization
system
allowed
obtain
TOFs
ca.
260,000
h−1.
addition
some
additives
able
reduce
possible
deactivation
increase
TOF
15%.
best
positive
results
were
obtained
by
adding
reducing
agents
such
ferrocene,
which
leads
higher
than
300,000
Language: Английский
Electrocyclization for the Synthesis of Mono‐ and Disulfonyl‐substituted Pyrazoles From Sulfonyl Hydrazines and 1,3‐Diketones
Yuanyuan Wu,
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Qiping Liu,
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Zhitao Ning
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et al.
ChemistrySelect,
Journal Year:
2024,
Volume and Issue:
9(45)
Published: Nov. 26, 2024
Abstract
The
tunable
electrocyclic
reactions
for
the
synthesis
of
a
series
mono‐
and
disulfonyl‐substituted
pyrazoles
from
sulfonyl
hydrazines
1,3‐diketones
were
investigated
by
utilizing
inexpensive
electrolytes
under
electrochemical
conditions
in
an
undivided
cell.
When
n
Bu
4
NBF
was
used
as
electrolyte,
it
afforded
monosulfonyl‐substituted
pyrazoles.
By
contrast,
when
NH
I
gave
mechanistic
investigation
shows
that
they
all
underwent
free
radical
process
but
formed
N
‐centered
hydrazine
S‐centered
pyrazoles,
respectively.
Language: Английский