Chemical Communications,
Год журнала:
2023,
Номер
59(56), С. 8719 - 8722
Опубликована: Янв. 1, 2023
Substituted
organoselenium
compounds
are
crucial
structural
motifs
in
pharmaceutical
molecules.
Herein,
we
report
a
metal,
oxidant,
and
base-free
electrochemical
approach
to
access
3-selenylindoles
through
an
oxidative
cyclization
of
2-alkynylanilines
with
diselenides.
This
environmentally
friendly
demonstrates
wide
range
substrate
scope
under
mild
reaction
conditions
undivided
cell
setup.
Chemical Reviews,
Год журнала:
2021,
Номер
122(2), С. 2752 - 2906
Опубликована: Авг. 10, 2021
Photoinduced
chemical
transformations
have
received
in
recent
years
a
tremendous
amount
of
attention,
providing
plethora
opportunities
to
synthetic
organic
chemists.
However,
performing
photochemical
transformation
can
be
quite
challenge
because
various
issues
related
the
delivery
photons.
These
challenges
barred
widespread
adoption
steps
industry.
past
decade,
several
technological
innovations
led
more
reproducible,
selective,
and
scalable
photoinduced
reactions.
Herein,
we
provide
comprehensive
overview
these
exciting
advances,
including
flow
chemistry,
high-throughput
experimentation,
reactor
design
scale-up,
combination
photo-
electro-chemistry.
Accounts of Chemical Research,
Год журнала:
2019,
Номер
53(1), С. 84 - 104
Опубликована: Дек. 19, 2019
To
improve
the
efficacy
of
molecular
syntheses,
researchers
wish
to
capitalize
upon
selective
modification
otherwise
inert
C-H
bonds.
The
past
two
decades
have
witnessed
considerable
advances
in
coordination
chemistry
that
set
stage
for
transformative
tools
functionalizations.
Particularly,
oxidative
C-H/C-H
and
C-H/Het-H
transformations
gained
major
attention
because
they
avoid
all
elements
substrate
prefunctionalization.
Despite
advances,
activations
been
dominated
by
precious
transition
metal
catalysts
based
on
palladium,
ruthenium,
iridium,
rhodium,
thus
compromising
sustainable
nature
overall
activation
approach.
same
holds
true
predominant
use
stoichiometric
chemical
oxidants
regeneration
active
catalyst,
prominently
featuring
hypervalent
iodine(III),
copper(II),
silver(I)
oxidants.
Thereby,
quantities
undesired
byproducts
are
generated,
which
preventive
applications
scale.
In
contrast,
elegant
merger
homogeneous
metal-catalyzed
with
electrosynthesis
bears
unique
power
achieve
outstanding
levels
oxidant
resource
economy.
Thus,
contrast
classical
electrosyntheses
control,
metalla-electrocatalysis
huge
largely
untapped
potential
unmet
site
selectivities
means
catalyst
control.
While
indirect
electrolysis
using
palladium
complexes
has
realized,
less
toxic
expensive
base
feature
distinct
beneficial
assets
toward
this
Account,
I
summarize
emergence
electrocatalyzed
earth-abundant
3d
metals
beyond,
a
topical
focus
contributions
from
our
laboratories
through
November
2019.
cobalt
electrocatalysis
was
identified
as
particularly
powerful
platform
wealth
transformations,
including
oxygenations
nitrogenations
well
alkynes,
alkenes,
allenes,
isocyanides,
carbon
monoxide,
among
others.
As
complementary
tools,
nickel,
copper,
very
recently
iron
devised
metalla-electrocatalyzed
activations.
Key
success
were
detailed
mechanistic
insights,
oxidation-induced
reductive
elimination
scenarios.
Likewise,
development
methods
make
weak
O-coordination
benefited
crucial
insights
into
catalyst's
modes
action
experiment,
operando
spectroscopy,
computation.
Overall,
thereby
syntheses
These
electrooxidative
frequently
characterized
improved
chemoselectivities.
Hence,
ability
dial
redox
at
minimum
level
required
desired
transformation
renders
an
ideal
functionalization
structurally
complex
molecules
sensitive
functional
groups.
This
strategy
was,
inter
alia,
successfully
applied
scale-up
continuous
flow
step-economical
assembly
polycyclic
aromatic
hydrocarbons.
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.
A
heterogeneous
catalyst
is
a
backbone
of
modern
sustainable
green
industries;
and
understanding
the
relationship
between
its
structure
properties
key
for
advancement.
Recently,
many
upscaling
synthesis
strategies
development
variety
respectable
control
atomically
precise
catalysts
are
reported
explored
various
important
applications
in
catalysis
energy
environmental
remediation.
Precise
atomic-scale
has
allowed
to
significantly
increase
activity,
selectivity,
some
cases
stability.
This
approach
proved
be
relevant
related
technologies
such
as
fuel
cell,
chemical
reactors
organic
synthesis,
Therefore,
this
review
aims
critically
analyze
recent
progress
on
single-atom
(SACs)
application
oxygen
reduction
reaction,
evolution
hydrogen
and/or
electrochemical
transformations.
Finally,
opportunities
that
may
open
up
future
summarized,
along
with
suggesting
new
possible
exploitation
SACs.
Journal of the American Chemical Society,
Год журнала:
2020,
Номер
142(37), С. 15678 - 15685
Опубликована: Авг. 31, 2020
Rhodium(III)-catalyzed
enantioselective
oxidative
C–H/C–H
cross-coupling
reaction
between
two
arenes
is
disclosed.
With
the
combination
of
a
chiral
CpRh(III)
complex
and
carboxylic
acid
additive,
direct
coupling
reactions
1-aryl
isoquinoline
derivatives
electron-rich
heteroarenes
such
as
thiophenes,
furans,
benzothiophenes,
benzofurans
are
realized
via
double
C–H
functionalization
process.
A
series
axially
compounds
obtained
in
excellent
yields
enantioselectivities
(up
to
99%
yield
ee).
Mechanistic
studies
suggest
that
both
bond
cleavages
may
not
be
turnover-limiting
step.