The
photoredox
eosin
Y-catalyzed
difunctionalization
of
alkenes
with
quinoxalinones
and
dialkyl
dithiophosphoric
acids
was
realized.
This
reaction
exhibited
excellent
functional
group
compatibility.
Journal of the American Chemical Society,
Journal Year:
2024,
Volume and Issue:
146(19), P. 13347 - 13355
Published: May 6, 2024
Azide
compounds
are
widely
present
in
natural
products
and
drug
molecules,
their
easy-to-transform
characteristics
make
them
used
the
field
of
organic
synthesis.
The
merging
transition-metal
catalysis
with
radical
chemistry
offers
a
versatile
platform
for
carboazidation
alkenes,
allowing
rapid
assembly
highly
functionalized
azides.
However,
direct
use
readily
available
hydrocarbon
feedstocks
as
sp
Organic Chemistry Frontiers,
Journal Year:
2024,
Volume and Issue:
11(14), P. 4024 - 4040
Published: Jan. 1, 2024
This
review
provides
a
comprehensive
overview
of
metal
catalysis
in
photo-electrochemical
systems,
discussing
reaction
mechanisms
and
offering
prospects
for
this
triadic
catalytic
mode.
The Journal of Organic Chemistry,
Journal Year:
2024,
Volume and Issue:
89(6), P. 4156 - 4164
Published: March 7, 2024
Metal
impurities
can
complicate
the
identification
of
active
catalyst
species
in
transition
metal
catalysis
and
electrocatalysis,
potentially
leading
to
misleading
findings.
This
study
investigates
influence
on
photocatalysis.
Specifically,
photocatalytic
reaction
inert
alkanes
using
chlorides
without
use
an
external
photocatalyst
was
studied,
achieving
successful
C(sp
Advanced Science,
Journal Year:
2024,
Volume and Issue:
11(29)
Published: June 3, 2024
Abstract
A
general
and
modular
protocol
is
reported
for
olefin
difunctionalization
through
mechanochemistry,
facilitated
by
cooperative
radical
ligand
transfer
(RLT)
electron
catalysis.
Utilizing
mechanochemical
force
catalytic
amounts
of
2,2,6,6‐tetramethylpiperidinyloxyl
(TEMPO),
ferric
nitrate
can
leverage
nitryl
radicals,
nitrooxy‐functional
group
via
RLT,
mediate
an
catalysis
cycle
under
room
temperature.
diverse
range
activated
unactivated
alkenes
exhibited
chemo‐
regioselective
1,2‐nitronitrooxylation
solvent‐free
or
solvent‐less
conditions,
showcasing
excellent
functional
tolerance.
Mechanistic
studies
indicated
a
significant
impact
mechanochemistry
highlighted
the
nature
this
nitrative
process.
Organic Chemistry Frontiers,
Journal Year:
2024,
Volume and Issue:
11(17), P. 4882 - 4894
Published: Jan. 1, 2024
This
review
focuses
on
the
synthesis
of
C–P
bonds
using
carbon-centered
radicals
with
phosphorous
compounds
different
valence
states
(P
III
,
P
V
4
)
under
photocatalysis.
Organic Chemistry Frontiers,
Journal Year:
2024,
Volume and Issue:
11(17), P. 4748 - 4756
Published: Jan. 1, 2024
Difunctionalizations
of
unactivated
olefins
with
fluoroalkyl
carboxylic
acids
or
aldehydes
via
a
radical-mediated
functional
group
migration
strategy
are
herein
reported.
ChemistrySelect,
Journal Year:
2025,
Volume and Issue:
10(4)
Published: Jan. 1, 2025
Abstract
Owing
to
its
possible
advantages
for
the
environment
and
economy,
photoredox
catalysis
of
organic
processes
fueled
by
iron
has
garnered
a
lot
interest
recently.
The
potential
photo‐induced
single‐electron
transfer
(SET)
events
occurring
outside
sphere
is
now
well
acknowledged.
Currently,
focus
shifted
newly
discovered
photoactivation
method
that
based
on
an
inner‐sphere
mode
reactivity
caused
population
visible‐light‐induced
homolysis
(VLIH)
states.
VLIH
activation,
in
contrast
photoredox,
specific
complexes,
offers
distinct
profiles,
does
not
require
redox
potentials
coincide.
These
attractive
properties
have
prompted
development
strategies
use
this
blueprint
manufacture
highly
reactive
open‐shell
species
mild
environments.
purpose
contribution
promote
novel
synthetic
techniques
sustainable
chemical
transformations
offer
educational
instrument
understanding
evolving
idea.