The Journal of Organic Chemistry,
Год журнала:
2024,
Номер
89(6), С. 4145 - 4155
Опубликована: Фев. 28, 2024
The
environmental
benefits
of
molecular
oxygen
as
the
oxidizing
agent
in
oxidation
reactions
that
synthesize
fine
chemicals
cannot
be
overstated.
Increased
interest
developing
robust
photocatalysts
is
stimulated
by
fact
current
photocatalytic
transformation
boom
has
made
previously
inaccessible
synthetic
approaches
possible.
Motivated
enzymatic
catalysis,
employing
a
reusable
phenalenyl-based
photocatalyst,
we
have
successfully
developed
oxidative
dehydrogenation
utilizing
greener
oxidant.
Under
photoinduced
conditions,
different
types
saturated
N-heterocycles
and
alcohols
were
dehydrogenated.
versatility
this
bioinspired
protocol
demonstrated
wide
variety
N-heteroaromatics,
such
quinoline,
carbazole,
quinoxaline,
acridine,
indole
derivatives,
well
aldehydes
ketones,
synthesized.
Detailed
mechanistic
studies
validate
proposed
mechanism.
Fluorescence
lifetime
CV
experiments
revealed
crucial
role
water
on
efficiency
reaction.
present
also
provides
chemoselectivity
scalability,
leading
to
superior
results
allowing
for
functionalization
bioactive
molecules
at
late
stage
sustainable
manner.
Chemical Society Reviews,
Год журнала:
2024,
Номер
53(14), С. 7455 - 7488
Опубликована: Янв. 1, 2024
Seawater
electrolysis
for
the
production
of
fuels
and
chemicals
involved
in
onshore
offshore
plants
powered
by
renewable
energies
offers
a
promising
avenue
unique
advantages
energy
environmental
sustainability.
Nevertheless,
seawater
presents
long-term
challenges
issues,
such
as
complex
composition,
potential
side
reactions,
deposition
poisoning
microorganisms
metal
ions,
well
corrosion,
thus
hindering
rapid
development
technology.
This
review
focuses
on
value-added
(hydrogen
beyond)
fine
through
electrolysis,
step
towards
sustainable
carbon
neutrality.
The
principle
related
are
first
introduced,
redox
reaction
mechanisms
summarized.
Strategies
operating
anodes
cathodes
including
application
chloride-
impurity-resistant
electrocatalysts/membranes
reviewed.
We
comprehensively
summarize
(hydrogen,
monoxide,
sulfur,
ammonia,
Nature Communications,
Год журнала:
2024,
Номер
15(1)
Опубликована: Март 30, 2024
Abstract
Herein,
we
report
an
electroreduction
of
unactivated
alkyl
alkenes
enabled
by
[Fe]-H,
which
is
provided
through
the
combination
anodic
iron
salts
and
silane
generated
in
situ
via
cathodic
reduction,
using
H
2
O
as
H-source.
The
catalytic
amounts
Si-additive
work
H-carrier
from
to
generate
a
highly
active
species
under
continuous
electrochemical
conditions.
This
approach
shows
broad
substrate
scope
good
functional
group
compatibility.
In
addition
hydrogenation,
use
D
instead
provides
desired
deuterated
products
yields
with
excellent
D-incorporation
(up
>99%).
Further
late-stage
hydrogenation
complex
molecules
drug
derivatives
demonstrate
potential
application
pharmaceutical
industry.
Mechanistic
studies
are
performed
provide
support
for
proposed
mechanistic
pathway.
Chinese Journal of Chemistry,
Год журнала:
2023,
Номер
42(10), С. 1145 - 1156
Опубликована: Дек. 26, 2023
Comprehensive
Summary
The
deuteration
of
organic
compounds
has
attracted
more
attentions
in
recent
years
for
the
potential
applications
new
drug
discovery
and
synthetic
chemistry.
For
this
purpose,
many
efficient
deuterium
labeling
methodologies
have
been
developed,
including
hydrogen
isotope
exchange
(HIE),
reductive
deuteration,
dehalogenative
that
allow
synthesis
selectively
deuterated
compounds.
In
last
few
years,
great
breakthroughs
selective
achieved
interest
molecules
is
rising.
review,
we
summarized
developments
since
2021.
Several
types
key
processes
incorporation
reactions,
H/D
exchange,
are
introduced
discussed.
Key
Scientists
2000s,
Derdau
Atzrodt's
group
made
contributions
to
directing
assisted
noble‐metal
catalyzed
arenes
labeled
During
same
period,
Sajiki
co‐workers
completed
a
series
reactions
by
heterogeneous
platinum‐group
metal
catalysts.
Since
2015,
Gregory
Pieters
developed
ruthenium
catalysts
exchange.
2016,
Chirik's
presence
homogeneous
iron
complex.
David
MacMillan
coworkers
photocatalyzed
HIE
α‐amino
C(sp
3
)–H
bonds.
From
2020,
nanoelectrodes
were
designed
deuterations
unactivated
unsaturated
bonds
Zhang's
group.
Recently,
Beller's
several
strategies
isotopic
using
earth‐abundant
Our
review
latest
important
Angewandte Chemie International Edition,
Год журнала:
2023,
Номер
62(44)
Опубликована: Сен. 14, 2023
Herein,
an
electrochemically
driven
NiH-catalyzed
reductive
coupling
of
alkyl
halides
and
alkenes
for
the
construction
Csp3
-Csp3
bonds
is
firstly
reported.
Notably,
serve
dual
function
as
substrates
hydrogen
sources
to
generate
NiH
species
under
electrochemical
conditions.
The
tunable
nature
this
reaction
realized
by
introducing
intramolecular
coordinating
group
substrate,
where
product
can
be
easily
adjusted
give
desired
branched
products.
method
proceeds
mild
conditions,
exhibits
a
broad
substrate
scope,
affords
moderate
excellent
yields
with
over
70
examples,
including
late-stage
modification
natural
products
drug
derivatives.
Mechanistic
insights
offer
evidence
process.
sp3
-carbon-halogen
activated
through
single
electron
transfer
(SET)
nickel
catalyst
in
its
low
valence
state,
generated
cathodic
reduction,
generation
from
pivotal
transformation.
Nature Communications,
Год журнала:
2024,
Номер
15(1)
Опубликована: Май 7, 2024
Herein,
we
develop
a
straightforward,
metal-free,
and
acid-/base-free
electrochemical
C4-selective
C
-
H
deuteration
of
pyridine
derivatives
with
economic
convenient
D
Nature Communications,
Год журнала:
2024,
Номер
15(1)
Опубликована: Июнь 19, 2024
Abstract
The
high
Faradaic
efficiency
(FE)
of
the
electrocatalytic
deuteration
organics
with
D
2
O
at
a
large
current
density
is
significant
for
deuterated
electrosynthesis.
However,
FE
and
are
two
ends
seesaw
because
severe
evolution
side
reaction
nearly
industrial
densities.
Herein,
we
report
combined
scenario
nanotip-enhanced
electric
field
surfactant-modified
interface
microenvironment
to
enable
arylacetonitrile
in
an
80%
−100
mA
cm
−2
.
increased
concentration
low
activation
energy
due
along
tips
accelerated
transfer
suppressed
by
surfactant-created
deuterophobic
contribute
breaking
trade-off
between
density.
Furthermore,
application
our
strategy
other
reactions
improved
efficiencies
rationalizes
design
concept.
Organic Chemistry Frontiers,
Год журнала:
2024,
Номер
unknown
Опубликована: Янв. 1, 2024
This
study
describes
a
pioneering
visible-light-induced
phosphine-catalyzed
halogen-atom
transfer
(XAT)
strategy
that
heralds
new
era
in
the
difunctionalization
of
[1.1.1]propellane.
Green Chemistry,
Год журнала:
2024,
Номер
26(14), С. 8315 - 8322
Опубликована: Янв. 1, 2024
A
photoelectrochemical
approach
for
the
carboacylation/silanoylation
of
alkenes
with
alkanes/hydrosilanes
is
described.
The
method
offers
a
new
perspective
chemists
to
rapidly
obtain
various
ketones
high
levels
structural
complexity.
Angewandte Chemie International Edition,
Год журнала:
2024,
Номер
63(22)
Опубликована: Март 20, 2024
Olefin
hydrogenation
is
one
of
the
most
important
transformations
in
organic
synthesis.
Electrochemical
transition
metal-catalyzed
an
attractive
approach
to
replace
dangerous
hydrogen
gas
with
electrons
and
protons.
However,
this
reaction
poses
major
challenges
due
rapid
evolution
(HER)
metal-hydride
species
that
outcompetes
alkene
step,
facile
deposition
metal
catalyst
at
electrode
stalls
reaction.
Here
we
report
economical
efficient
strategy
achieve
high
selectivity
for
reactivity
over
well-established
HER.
Using
inexpensive
bench-stable
nickel
salt
as
catalyst,
mild
features
outstanding
substrate
generality
functional
group
compatibility,
distinct
chemoselectivity.
In
addition,
hydrodebromination
alkyl
aryl
bromides
could
be
realized
using
same
system
a
different
ligand,
chemoselectivity
between
achieved
through
ligand
selection.
The
practicability
our
method
has
been
demonstrated
by
success
large-scale
synthesis
catalytic
amount
electrolyte
minimal
solvent.
Cyclic
voltammetry
kinetic
studies
were
performed,
which
support
Ni
Organic Letters,
Год журнала:
2024,
Номер
26(21), С. 4427 - 4432
Опубликована: Май 17, 2024
2,3-Diaryl
propanoic
acids
are
important
structures
as
a
result
of
their
widespread
presence
in
numerous
bioactive
compounds.
However,
the
limitations
existing
synthetic
techniques
include
requirement
for
costly
catalysts
and
limited
substrates.
Here,
we
developed
novel
electroreductive
arylcarboxylation
alkenes
with
CO2
based
on
radical–polar
crossover
pathway
assisted
by
easily
accessible
dimethyl
terephthalate
reductive
mediator.
This
method
will
provide
an
efficient
strategy
synthesis
2,3-diarylpropanoic
acids.