Organic Letters,
Год журнала:
2018,
Номер
20(23), С. 7396 - 7399
Опубликована: Ноя. 21, 2018
The
directly
external
oxidant-free
oxytrifluoromethylation
and
aminotrifluoromethylation
of
alkenes
have
been
developed
through
the
constant
current
electrolysis
synergizing
with
a
Lewis-acid
catalysis
protocol.
By
using
sodium
trifluoromethanesulfinate
as
trifluoromethyl
source,
method
enabled
difunctionalization
C-C
double
bonds
wide
range
styrene
derivatives.
Chemical Society Reviews,
Год журнала:
2018,
Номер
47(15), С. 5786 - 5865
Опубликована: Янв. 1, 2018
This
review
provides
an
overview
of
the
use
electrochemistry
as
appealing
platform
for
expediting
carbon–hydrogen
functionalization
and
carbon–nitrogen
bond
formation.
Chemical Society Reviews,
Год журнала:
2021,
Номер
50(14), С. 7941 - 8002
Опубликована: Янв. 1, 2021
Electrochemistry
has
recently
gained
increased
attention
as
a
versatile
strategy
for
achieving
challenging
transformations
at
the
forefront
of
synthetic
organic
chemistry.
Electrochemistry's
unique
ability
to
generate
highly
reactive
radical
and
ion
intermediates
in
controlled
fashion
under
mild
conditions
inspired
development
number
new
electrochemical
methodologies
preparation
valuable
chemical
motifs.
Particularly,
recent
developments
electrosynthesis
have
featured
an
use
redox-active
electrocatalysts
further
enhance
control
over
selective
formation
downstream
reactivity
these
intermediates.
Furthermore,
electrocatalytic
mediators
enable
proceed
manner
that
is
mechanistically
distinct
from
purely
methods,
allowing
subversion
kinetic
thermodynamic
obstacles
encountered
conventional
synthesis.
This
review
highlights
key
innovations
within
past
decade
area
electrocatalysis,
with
emphasis
on
mechanisms
catalyst
design
principles
underpinning
advancements.
A
host
oxidative
reductive
are
discussed
grouped
according
classification
transformation
nature
electrocatalyst.
Angewandte Chemie International Edition,
Год журнала:
2019,
Номер
59(1), С. 74 - 108
Опубликована: Май 22, 2019
Abstract
Radical–radical
couplings
are
mostly
nearly
diffusion‐controlled
processes.
Therefore,
the
selective
cross‐coupling
of
two
different
radicals
is
challenging
and
not
a
synthetically
valuable
transformation.
However,
if
have
lifetimes
they
generated
at
equal
rates,
will
become
dominant
process.
This
high
cross‐selectivity
based
on
kinetic
phenomenon
called
persistent
radical
effect
(PRE).
In
this
Review,
an
explanation
PRE
supported
by
simulations
simple
model
systems
provided.
Radical
stabilities
discussed
within
context
their
lifetimes,
various
examples
PRE‐mediated
radical–radical
in
synthesis
summarized.
It
shown
that
restricted
to
coupling
with
transient
radical.
If
one
partner
longer‐lived
than
other
radical,
operates
achieved.
important
point
expands
scope
chemistry.
The
Review
divided
into
parts,
namely
1)
or
organic
2)
“radical–metal
crossover
reactions”;
here,
metal‐centered
species
more
generally
transition‐metal
complexes
able
react
discussed—a
field
has
flourished
recently.
Accounts of Chemical Research,
Год журнала:
2020,
Номер
53(3), С. 547 - 560
Опубликована: Фев. 20, 2020
Electrochemistry
has
been
used
as
a
tool
to
drive
chemical
reactions
for
over
two
centuries.
With
the
help
of
an
electrode
and
power
source,
chemists
are
bestowed
with
imaginary
reagent
whose
potential
can
be
precisely
dialed
in.
The
theoretically
infinite
redox
range
renders
electrochemistry
capable
oxidizing
or
reducing
some
most
tenacious
compounds
(e.g.,
F
ACS Central Science,
Год журнала:
2020,
Номер
6(8), С. 1317 - 1340
Опубликована: Июль 16, 2020
As
the
breadth
of
radical
chemistry
grows,
new
means
to
promote
and
regulate
single-electron
redox
activities
play
increasingly
important
roles
in
driving
modern
synthetic
innovation.
In
this
regard,
photochemistry
electrochemistry-both
considered
as
niche
fields
for
decades-have
seen
an
explosive
renewal
interest
recent
years
gradually
have
become
a
cornerstone
organic
chemistry.
Outlook
article,
we
examine
current
state-of-the-art
areas
electrochemistry
photochemistry,
well
nascent
area
electrophotochemistry.
These
techniques
employ
external
stimuli
activate
molecules
imbue
privileged
control
reaction
progress
selectivity
that
is
challenging
traditional
chemical
methods.
Thus,
they
provide
alternative
entries
known
reactive
intermediates
enable
distinct
strategies
were
previously
unimaginable.
Of
many
hallmarks,
electro-
are
often
classified
"green"
technologies,
promoting
reactions
under
mild
conditions
without
necessity
potent
wasteful
oxidants
reductants.
This
reviews
most
growth
these
with
special
emphasis
on
conceptual
advances
given
rise
enhanced
accessibility
tools
trade.
Chemical Reviews,
Год журнала:
2021,
Номер
122(2), С. 2487 - 2649
Опубликована: Ноя. 9, 2021
Redox
processes
are
at
the
heart
of
synthetic
methods
that
rely
on
either
electrochemistry
or
photoredox
catalysis,
but
how
do
and
catalysis
compare?
Both
approaches
provide
access
to
high
energy
intermediates
(e.g.,
radicals)
enable
bond
formations
not
constrained
by
rules
ionic
2
electron
(e)
mechanisms.
Instead,
they
1e
mechanisms
capable
bypassing
electronic
steric
limitations
protecting
group
requirements,
thus
enabling
chemists
disconnect
molecules
in
new
different
ways.
However,
while
providing
similar
intermediates,
differ
several
physical
chemistry
principles.
Understanding
those
differences
can
be
key
designing
transformations
forging
disconnections.
This
review
aims
highlight
these
similarities
between
comparing
their
underlying
principles
describing
impact
electrochemical
photochemical
methods.
Chemical Reviews,
Год журнала:
2021,
Номер
122(3), С. 3180 - 3218
Опубликована: Ноя. 19, 2021
Synthetic
organic
electrosynthesis
has
grown
in
the
past
few
decades
by
achieving
many
valuable
transformations
for
synthetic
chemists.
Although
electrocatalysis
been
popular
improving
selectivity
and
efficiency
a
wide
variety
of
energy-related
applications,
last
two
decades,
there
much
interest
to
develop
conceptually
novel
transformations,
selective
functionalization,
sustainable
reactions.
This
review
discusses
recent
advances
combination
electrochemistry
homogeneous
transition-metal
catalysis
synthesis.
The
enabling
mechanistic
studies
are
presented
alongside
advantages
as
well
future
directions
address
challenges
metal-catalyzed
electrosynthesis.
Journal of the American Chemical Society,
Год журнала:
2018,
Номер
140(25), С. 7913 - 7921
Опубликована: Май 29, 2018
Electrochemical
oxidative
C–H/N–H
activations
have
been
accomplished
with
a
versatile
cobalt
catalyst
in
terms
of
[4
+
2]
annulations
internal
alkynes.
The
electro-oxidative
C–H
activation
manifold
proved
viable
an
undivided
cell
setup
under
exceedingly
mild
reaction
conditions
at
room
temperature
using
earth-abundant
catalysts.
electrochemical
catalysis
prevents
the
use
transition
metal
oxidants
catalysis,
generating
H2
as
sole
byproduct.
Detailed
mechanistic
studies
provided
strong
support
for
facile
cobaltation
by
initially
formed
cobalt(III)
catalyst.
subsequent
alkyne
migratory
insertion
was
interrogated
mass
spectrometry
and
DFT
calculations,
providing
formation
key
seven-membered
cobalta(III)
cycle
regioselective
fashion.
Key
to
success
unprecedented
alkynes
represented
N-2-pyridylhydrazides,
which
we
developed
traceless
electrocleavage
strategy
electroreductive
samarium
temperature.