Green Chemistry,
Год журнала:
2023,
Номер
25(7), С. 2681 - 2689
Опубликована: Янв. 1, 2023
Herein,
a
straightforward
route
for
dual
α,β-C(sp
3
)–H
functionalized
cyclic
N
-aryl
amines
using
combination
of
electrocatalysis
and
iron
catalysis
is
disclosed,
setting
the
stage
challenging
multiple
site
selective
C–H
functionalization.
Angewandte Chemie International Edition,
Год журнала:
2022,
Номер
62(3)
Опубликована: Ноя. 16, 2022
Herein,
a
direct,
metal-free,
and
site-selective
electrochemical
C-H
carboxylation
of
arenes
by
reductive
activation
using
CO2
as
the
economic
abundant
carboxylic
source
was
reported.
The
electrocarboxylation
carried
out
in
an
operationally
simple
manner
with
high
chemo-
regioselectivity,
setting
stage
for
challenging
unactivated
(hetero)arenes.
robust
nature
strategy
reflected
broad
scope
substrates
excellent
atom
economy
unique
selectivity.
Notably,
direct
selective
various
worked
well
this
approach,
including
electron-deficient
naphthalenes,
pyridines,
phenyl
derivatives,
substituted
quinolines.
method
benefits
from
being
externally
catalyst-free,
metal-free
base-free,
which
makes
it
extremely
attractive
potential
applications.
Green Chemistry,
Год журнала:
2023,
Номер
25(8), С. 3095 - 3102
Опубликована: Янв. 1, 2023
A
regiodivergent
electrochemical
defluorocarboxylation
of
gem
-difluorocyclopropanes
is
realized,
providing
access
to
branched
and
linear
carboxylated
monofluorinated
alkenes.
Journal of the American Chemical Society,
Год журнала:
2024,
Номер
146(21), С. 14864 - 14874
Опубликована: Май 16, 2024
The
exploitation
of
carbon
dioxide
(CO2)
as
a
sustainable,
plentiful,
and
harmless
C1
source
for
the
catalytic
synthesis
enantioenriched
carboxylic
acids
has
long
been
acknowledged
pivotal
task
in
synthetic
chemistry.
Herein,
we
present
current-driven
nickel-catalyzed
reductive
carboxylation
reaction
with
CO2
fixation,
facilitating
formation
C(sp3)–C(sp2)
bonds
by
circumventing
handling
moisture-sensitive
organometallic
reagents.
This
electroreductive
protocol
serves
practical
platform,
paving
way
propargylic
(up
to
98%
enantiomeric
excess)
from
racemic
carbonates
CO2.
efficacy
this
transformation
is
exemplified
its
successful
utilization
asymmetric
total
(S)-arundic
acid,
(R)-PIA,
(S)-chizhine
D,
(S)-cochlearin
G,
(S,S)-alexidine,
thereby
underscoring
potential
electrosynthesis
achieve
complex
molecular
architectures
sustainably.
Angewandte Chemie International Edition,
Год журнала:
2024,
Номер
63(22)
Опубликована: Март 26, 2024
Abstract
Upgrading
CO
2
to
value‐added
chiral
molecules
via
catalytic
asymmetric
C−C
bond
formation
is
a
highly
important
yet
challenging
task.
Although
great
progress
on
the
of
centrally
carboxylic
acids
has
been
achieved,
construction
axially
with
never
reported
date.
Herein,
we
report
first
synthesis
,
which
enabled
by
nickel‐catalyzed
dynamic
kinetic
reductive
carboxylation
racemic
aza‐biaryl
triflates.
A
variety
acids,
are
valuable
but
difficult
obtain
catalysis,
generated
in
an
enantioconvergent
version.
This
new
methodology
features
good
functional
group
tolerance,
easy
scale‐up,
facile
transformation
and
avoids
cumbersome
steps,
handling
organometallic
reagents
using
stoichiometric
materials.
Mechanistic
investigations
indicate
process
induced
nickel
catalysis.
Arabian Journal of Chemistry,
Год журнала:
2024,
Номер
17(8), С. 105822 - 105822
Опубликована: Май 24, 2024
Owing
to
the
environmental
and
energy
problems
nowadays,
one
of
enormous
challenges
is
expanding
clean,
renewable
reduce
destructive
ecological
effects
chemical
industries.
Compared
with
other
traditional
processes,
electrochemical
method
has
some
benefits,
such
as
being
selective,
causing
minor
waste,
working
under
mild
conditions
no
external
oxidizing
or
reducing
reagents,
making
this
approach
more
economical
eco-friendly.
Electrochemistry
represents
a
powerful
tool
within
synthetic
organic
chemistry.
The
development
part
chemistry
intends
performance
reactions
employing
electrons,
including
adding
removing
electrons.
Using
electric
current
reagent
advantages,
simplicity
reactions,
accessibility
materials,
replacing
toxic
applying
an
eco-friendly
environment.
During
last
decades,
there
been
much
effort
decrease
usage
fossil
fuels,
electricity
emerged
common
source.
conversion
into
leads
new
paths,
naturally
safe
environmentally
friendly.
Developing
electrochemistry
approaches
for
performing
high-performance
essential
reaction
green
strategy
because
utilization
instead
stoichiometric
oxidants
reductants.
Due
its
helpful
friendly
ability
produce
reactive
intermediates,
advanced
considerably
in
oxidative
hydrogen
evolution
coupling
sacrificial
anode
electroreduction.
New
developments
focus
on
developing
electrolytic
catalysts,photoelectrocatalysis,
bioelectrosynthesis,
optimizing
electrode
paired
electrolysis,
artificial
intelligence-assisted
electrosynthesis.
Thus,
daily
significant
number
construction
projects
possibilities
electrochemistry.
Electrochemical
methods
constructing
compounds
have
tolerated
renewal
past
decades.
Organic
wealthy
background
synthesis.
We
hope
review
helps
attract
attention
from
researchers
by
using
processes
laboratory
industrial
centers,
which
pollution
create
In
review,
organohalides
synthesizing
various
products
summarized
discussed
since
2000.
Organic Letters,
Год журнала:
2024,
Номер
26(15), С. 3241 - 3246
Опубликована: Апрель 5, 2024
Herein,
we
report
an
electrochemical
protocol
for
the
dicarboxylation
of
aryl
alkynes
using
CO2.
With
a
graphite
rod
as
cathode
and
Al
sacrificial
anode,
series
valuable
butenedioic
acids
are
obtained
in
moderate
to
excellent
yields
with
E/Z
ratio
up
50:1.
This
method
features
high
E-selectivity,
step
atom
economy,
easy
scalability,
nice
substrate
scope,
which
renders
it
appealing
promising
applications
organic
synthesis
materials
chemistry.
Chemical Society Reviews,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 1, 2025
This
review
highlights
organo-mediators
that
enable
electrochemical
reactions
via
outer-sphere
electron
transfer
(ET),
offering
advantages
such
as
availability,
tunability,
and
simplified
post-processing
compared
to
direct
electrolysis.