Journal of the American Chemical Society,
Год журнала:
2021,
Номер
143(23), С. 8597 - 8602
Опубликована: Июнь 2, 2021
A
method
for
C–H
bond
amination
via
an
electrophotocatalytic
Ritter-type
reaction
is
described.
The
catalyzed
by
a
trisaminocyclopropenium
(TAC)
ion
in
electrochemical
cell
under
irradiation.
These
conditions
convert
benzylic
bonds
to
acetamides
without
the
use
of
stoichiometric
chemical
oxidant.
range
functionality
shown
be
compatible
with
this
transformation,
and
several
complex
substrates
are
demonstrated.
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.
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(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.
Green Chemistry,
Год журнала:
2020,
Номер
22(11), С. 3358 - 3375
Опубликована: Янв. 1, 2020
This
tutorial
bridges
an
important
knowledge
gap
by
providing
easily
accessible
introduction
that
enables
synthetic
chemists
to
explore
electrochemistry.
Journal of the American Chemical Society,
Год журнала:
2020,
Номер
142(41), С. 17693 - 17702
Опубликована: Сен. 17, 2020
The
selective
installation
of
azide
groups
into
C(sp3)-H
bonds
is
a
priority
research
topic
in
organic
synthesis,
particularly
pharmaceutical
discovery
and
late-stage
diversification.
Herein,
we
demonstrate
generalized
manganese-catalyzed
oxidative
azidation
methodology
using
nucleophilic
NaN3
as
an
source
under
electrophotocatalytic
conditions.
This
approach
allows
us
to
perform
the
reaction
without
necessity
adding
excess
substrate
successfully
avoiding
use
stoichiometric
chemical
oxidants
such
iodine(III)
reagent
or
NFSI.
A
series
tertiary
secondary
benzylic
C(sp3)-H,
aliphatic
drug-molecule-based
substrates
are
well
tolerated
our
protocol.
simultaneous
gram-scale
synthesis
ease
transformation
amine
collectively
advocate
for
potential
application
preparative
synthesis.
Good
reactivity
bond
selectivity
incorporate
nitrogen-based
functionality
at
alkyl
group
also
provide
opportunities
manipulate
numerous
medicinal
candidates.
We
anticipate
synthetic
protocol,
consisting
metal
catalysis,
electrochemistry,
photochemistry,
would
new
sustainable
option
execute
challenging
transformations.