The Journal of Organic Chemistry,
Год журнала:
2024,
Номер
unknown
Опубликована: Ноя. 22, 2024
A
photocatalytic
decyanative
C(sp3)–H
pyridination
of
dihydroquinoxalin-2-ones
with
4-cyanopyridines
was
developed
by
utilizing
4CzIPN
as
the
photocatalyst.
Mechanism
studies
show
that
this
organophotocatalytic
direct
undergoes
a
radical–radical
cross-coupling
pathway
promoted
consecutive
photoinduced
electron
transfer.
The Journal of Organic Chemistry,
Год журнала:
2025,
Номер
90(4), С. 1656 - 1662
Опубликована: Янв. 21, 2025
We
report
a
photoredox-catalyzed
three-component
sulfonaminoalkynylation
of
alkenes
with
N-aminopyridine
salts
and
potassium
alkynyltrifluoroborate
salts.
This
aminoalkylation
reaction
underwent
radial/polar
crossover
mechanism,
which
was
distinguished
from
the
previous
reports.
A
variety
β-alkynylated
sulfonamides
were
obtained
in
moderate
to
excellent
yields.
The
versatility
this
method
further
evidenced
by
its
successful
application
modifying
biological
molecules
advanced
stages
development.
The Journal of Organic Chemistry,
Год журнала:
2025,
Номер
unknown
Опубликована: Фев. 20, 2025
Polymer-supported
selenium
has
been
reported
as
a
heterogeneous
catalyst
that
is
easily
separated
from
the
reaction
system,
thereby
making
recovery
and
reuse
of
more
convenient.
However,
utilization
polymer-supported
in
preparation
catalysts
not
restricted
to
aforementioned
technical
advantages.
Recent
studies
have
shown
small-molecule
organoselenium
significant
performance
differences,
leading
distinct
mechanisms,
which
offer
opportunities
for
development
new
organic
reactions.
The Journal of Organic Chemistry,
Год журнала:
2025,
Номер
unknown
Опубликована: Фев. 26, 2025
The
first
example
of
heterogeneous
photoredox-catalyzed
fluoroalkylation
4H-pyrido[1,2-a]pyrimidin-4-ones
has
been
developed.
With
low-cost
commercial
g-C3N4
as
the
recyclable
photocatalyst
and
cheap
sodium
fluoroalkyl
sulfonates
source,
a
variety
fluoroalkylated
pyridopyrimidinones
were
constructed
in
moderate
to
high
yields.
present
reaction
can
be
easily
scaled
up
with
good
efficiency,
catalytic
system
reused
5
times
slight
loss
activities.
Furthermore,
biological
activity
synthesized
compounds
was
preliminarily
investigated.
The Journal of Organic Chemistry,
Год журнала:
2024,
Номер
unknown
Опубликована: Ноя. 25, 2024
Herein,
the
first
example
of
self-catalyzed
sono-photoinduced
carbon-carbon
bond
formation
was
described.
Combining
advantages
phototriggered
self-catalysis
and
ultrasonic
catalysis,
a
wide
range
3-arylquinoxalin-2(1
A
100%
atom
economical
construction
of
hydroxyalkylated
N-heteroarenes
through
decatungstate-catalyzed
tandem
cyclization/self-hydrogenation
isocyanides
and
aldehydes
under
exogenous
hydrogen
reagent-
byproduct-free
conditions
was
developed.
Asian Journal of Organic Chemistry,
Год журнала:
2024,
Номер
unknown
Опубликована: Окт. 27, 2024
Abstract
With
Ag/g‐C
3
N
4
semiconductor
as
the
heterogeneous
photocatalyst,
visible
light
promoted
synthesis
of
unsymmetric
diaryl
chalcogenides
could
be
achieved
under
additive‐free
and
mild
conditions.
A
series
were
generated
in
good
to
excellent
yields
with
high
functional
group
tolerance.
The
photocatalyst
is
easily
recovered
from
reaction
mixture
reused
at
least
5
times,
opening
way
for
larger‐scale
industrial
applications
this
type
photocatalytic
bond‐forming
reactions.