Unlocking the Potential of Oxidative Asymmetric Catalysis with Continuous Flow Electrochemistry
Journal of the American Chemical Society,
Год журнала:
2024,
Номер
146(11), С. 7178 - 7184
Опубликована: Март 11, 2024
In
the
field
of
catalytic
asymmetric
synthesis,
less-treated
path
lies
in
oxidative
transformations.
The
hurdles
pinpointing
appropriate
chemical
oxidants
and
addressing
their
compatibility
issues
with
catalysts
functionalities
present
significant
challenges.
Organic
electrochemistry,
employing
traceless
electrons
for
redox
reactions,
is
underscored
as
a
promising
solution.
However,
commonly
used
electrolysis
batch
cells
introduces
its
own
set
challenges,
hindering
advancement
electrochemical
catalysis.
Here
we
introduce
microfluidic
electrochemistry
platform
single-pass
continuous
flow
reactors
that
exhibits
wide-ranging
applicability
to
various
This
exemplified
through
sulfenylation
1,3-dicarbonyls,
dehydrogenative
C–C
coupling,
alkene
annulation
processes.
unique
properties
not
only
eliminate
need
but
also
enhance
reaction
efficiency
reduce
use
additives
electrolytes.
These
salient
features
expedite
discovery
development
addition,
production
facilitated
by
parallel
ensures
straightforward
upscaling,
removing
necessity
reoptimization
across
scales,
evidenced
direct
translation
from
milligram
screening
hectogram
synthesis.
Язык: Английский
A Comprehensive Review of Magnetic Nanocatalysts for C−S, C−Se Bond Formation
ChemistryOpen,
Год журнала:
2025,
Номер
unknown
Опубликована: Март 27, 2025
Abstract
This
review
manuscript
examines
magnetic
nanocatalysts
and
their
pivotal
role
in
forming
carbon‐sulfur
(C−S)
carbon‐selenium
(C−Se)
bonds.
The
study
delves
into
the
latest
advancements
synthesis,
characterization,
application
of
nanocatalysts,
highlighting
unique
advantages,
including
enhanced
catalytic
activity,
superior
selectivity,
easy
recovery
through
separation,
which
align
with
principles
green
chemistry.
Through
a
critical
analysis
recent
research
findings,
this
also
explores
mechanistic
pathways
facilitated
by
these
offering
insights
operational
efficiency
potential
for
recyclability.
aims
not
only
to
catalog
current
achievements
burgeoning
field
but
identify
challenges
propose
future
directions
developing
more
efficient,
sustainable,
versatile
systems
C−S
C−Se
bond
formation.
By
encompassing
broad
spectrum
ranging
from
bare
magnets
functionalized
composite
materials,
is
comprehensive
resource
researchers
engaged
organic
catalysis,
sustainable
Язык: Английский
Advances in Asymmetric Electrochemical Synthesis
Chinese Journal of Organic Chemistry,
Год журнала:
2024,
Номер
44(3), С. 673 - 673
Опубликована: Янв. 1, 2024
Язык: Английский
Iodine-mediated thio-arylation under electrochemical conditions
RSC Advances,
Год журнала:
2025,
Номер
15(15), С. 12042 - 12046
Опубликована: Янв. 1, 2025
An
efficient
iodine-mediated
electrochemical
construction
of
C–S
bonds
under
metal-free
and
chemical
oxidant-free
conditions.
Язык: Английский
Asymmetric Counteranion‐Directed Electrocatalysis for Enantioselective Control of Radical Cation
Zhenhui Xu,
Changdi Zheng,
Jie Lin
и другие.
Angewandte Chemie International Edition,
Год журнала:
2024,
Номер
64(1)
Опубликована: Авг. 30, 2024
The
control
of
enantioselectivity
in
radical
cation
reactions
presents
long-standing
challenges,
despite
a
few
successful
examples.
We
introduce
novel
strategy
asymmetric
counteranion-directed
electrocatalysis
to
address
chemistry.
This
concept
has
been
successfully
demonstrated
two
reactions:
an
dehydrogenative
indole-phenol
[3+2]
coupling
and
atroposelective
C-H/N-H
coupling.
These
have
enabled
the
synthesis
benzofuroindolines
C-N
axially
chiral
indoles
with
high
yields
excellent
enantiomeric
excesses.
Detailed
mechanistic
studies
confirmed
radical-radical
mechanism.
Moreover,
density
functional
theory
(DFT)
calculations
supported
indole
as
pivotal
intermediate,
rather
than
neutral
indolyl
radical,
shedding
new
light
on
underlying
processes
driving
these
reactions.
Язык: Английский
I2 or I2/PIFA one‒pot induced system for rapid synthesis of chalcogenated enamides, uracils or 2-pyridones under mild conditions
New Journal of Chemistry,
Год журнала:
2024,
Номер
48(28), С. 12793 - 12799
Опубликована: Янв. 1, 2024
An
I
2
-mediated
β-C(sp
)–H
chalcogenylation
of
enamides
under
mild
and
rapid
conditions
has
been
developed.
Sequential
addition
PIFA
led
to
valuable
5-thio-
5-seleno-2-pyridones
with
a
free
C3
position.
Язык: Английский
Electrochemical Nickel-Catalyzed Cross-Electrophile Coupling of Alkenyl Triflates with α-Chloroamides
Organic Letters,
Год журнала:
2024,
Номер
26(30), С. 6364 - 6369
Опубликована: Июль 25, 2024
Cross-electrophile
coupling
reactions
of
different
electrophiles
have
been
extensively
studied
but
mainly
limited
to
bromides
and
iodides.
Here,
we
report
an
electrochemically
induced
nickel-catalyzed
cross-electrophile
strategy
between
alkenyl
triflates
α-chloroamides
in
undivided
cell
under
mild
reaction
conditions,
affording
the
α-functionalized
amide
derivatives
good
excellent
yields
with
broad
substrate
scopes
functional
group
tolerance.
The
control
experiments
were
conducted,
a
plausible
mechanism
was
proposed.
Язык: Английский
Asymmetric Counteranion‐Directed Electrocatalysis for Enantioselective Control of Radical Cation
Zhenhui Xu,
Changdi Zheng,
Jie Lin
и другие.
Angewandte Chemie,
Год журнала:
2024,
Номер
137(1)
Опубликована: Авг. 30, 2024
Abstract
The
control
of
enantioselectivity
in
radical
cation
reactions
presents
long‐standing
challenges,
despite
a
few
successful
examples.
We
introduce
novel
strategy
asymmetric
counteranion‐directed
electrocatalysis
to
address
chemistry.
This
concept
has
been
successfully
demonstrated
two
reactions:
an
dehydrogenative
indole‐phenol
[3+2]
coupling
and
atroposelective
C−H/N−H
coupling.
These
have
enabled
the
synthesis
benzofuroindolines
C−N
axially
chiral
indoles
with
high
yields
excellent
enantiomeric
excesses.
Detailed
mechanistic
studies
confirmed
radical‐radical
mechanism.
Moreover,
density
functional
theory
(DFT)
calculations
supported
indole
as
pivotal
intermediate,
rather
than
neutral
indolyl
radical,
shedding
new
light
on
underlying
processes
driving
these
reactions.
Язык: Английский