Organic & Biomolecular Chemistry,
Год журнала:
2024,
Номер
unknown
Опубликована: Дек. 23, 2024
Herein,
we
report
a
novel
synthetic
method
for
isoxazolidine
derivatives
through
visible-light-induced
photoredox
cascade
cyclization
of
nitroarenes
with
triethylamine
under
aerobic
conditions.
Organic Letters,
Год журнала:
2024,
Номер
26(31), С. 6736 - 6741
Опубликована: Июль 29, 2024
A
visible-light-induced
photoredox
three-component
carbocyclization
reaction
of
1,7-enynes
with
sulfoxonium
ylides
and
water
is
reported.
The
protocol
provides
a
facile
entry
to
structurally
valuable
highly
functionalized
cyclopenta[c]quinoline
scaffolds
in
chemoselective
stereoselective
manner.
Salient
features
this
method
include
redox-neutral
conditions,
no
requirement
base
or
other
additive,
good
functional-group
tolerance.
Organic Letters,
Год журнала:
2024,
Номер
26(12), С. 2398 - 2402
Опубликована: Март 18, 2024
Herein,
we
introduce
a
tetralone-mediated
photocyclization
method
of
N-arylacrylamides.
The
protocol
proceeds
smoothly
to
deliver
diverse
set
3,4-dihydroquinolinones
in
moderate
good
yields
with
excellent
functional
group
compatibility
and
readily
allows
for
late-stage
modifications
number
complex
drug
molecules.
Mechanistic
studies
reveal
that
the
present
systems
ultraviolet
light
irradiation
enable
cyclization
via
energy
transfer
exclusive
1,3-hydrogen
shift.
Herein,
a
N-phenylphenothiazine-based
hyper-cross-linked
polymer
(PTH-HCP)
was
finely
designed
and
constructed,
which
serves
as
metal-free
heterogeneous
photocatalyst
for
organic
transformations.
Characterization
experiments
have
shown
that
this
demonstrates
outstanding
stability,
extensive
surface
area,
exceptional
photoelectric
response
properties.
Moreover,
PTH-HCP
showed
good
catalytic
efficiency
recyclability
in
the
photochemically
driven
difluoromethylation/cyclization
reactions.
This
work
provides
strategy
design
construction
of
photocatalysts
offers
support
their
broad
prospects
synthetic
applications.
Organic Chemistry Frontiers,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 1, 2025
We
reported
the
first
example
of
visible-light-induced
radical
cascade
cyclization
2-isocyanobiaryls
via
1,5-HAT,
which
is
characterized
by
broad
substrate
scope,
excellent
functional
group
compatibility
and
no
requirement
any
metals
base.
European Journal of Organic Chemistry,
Год журнала:
2024,
Номер
27(41)
Опубликована: Авг. 6, 2024
Abstract
A
visible‐light‐induced
photoredox‐catalyzed
radical
tandem
cyclization
of
o
‐isocyanodiaryl
amines
with
arylthiodifluoroalkyl
2‐pyridyl
sulfones
or
difluormethyl
bromides
has
been
realized
for
the
first
time.
The
reaction
works
a
broad
range
substrates
and
provides
simple
efficient
method
synthesis
11‐difluoromethyl‐substituted
dibenzodiazepines
from
easily
available
starting
materials
in
very
mild
conditions.
Chinese Journal of Chemistry,
Год журнала:
2024,
Номер
unknown
Опубликована: Сен. 10, 2024
Comprehensive
Summary
A
visible‐light‐induced
decarboxylative
radical
cascade
cyclization
reaction
between
N
‐(2‐cyanoaryl)‐acrylamides
and
alkyl
‐(acyloxy)phthalimide
(NHPI
esters)
for
the
construction
of
phenanthridine
derivatives
has
been
developed.
This
approach
utilizes
lithium
iodide
(LiI)
triphenylphosphine
(PPh
3
)
as
redox
catalysts
is
produced
through
photoactivation
electron
donor‐acceptor
(EDA)
complex.
series
primary,
secondary,
tertiary
alkyl‐substituted
phenanthridines
are
prepared
in
up
to
82%
yield
without
transition‐metal
catalysts,
chemical
oxidants,
or
metal‐/organic
dye‐based
photocatalysts.
Green Chemistry,
Год журнала:
2024,
Номер
26(21), С. 10804 - 10810
Опубликована: Янв. 1, 2024
We
present
an
efficient
and
sustainable
protocol
for
the
photoinduced-radical
hydrocyclization
of
isocyanides,
providing
a
united
route
to
assemble
diverse
α-unsubstituted
N-heteroarenes.
Organic Letters,
Год журнала:
2024,
Номер
26(36), С. 7707 - 7712
Опубликована: Авг. 28, 2024
Herein,
we
have
developed
a
complementary
entry
to
enable
hydroheteroarylation
of
alkenes
involving
basically
photoredox
dearomatizative
heterocyclic
carbon
radical
formation
through
acid-coupled
electron
transfer
followed
by
Giese
addition.
While
protonic
solvent
and
thiophenol
additive
enabled
two
molecular
hydroheteroarylations
alkenes,
the
nonproton
environment
with
BF
A
visible-light
induced
intermolecular
hydroamination
of
alkenes
with
azoles
is
reported,
delivering
pharmaceutically
valuable
N-benzyl
in
high
yields
excellent
Markovnikov
selectivity.
Mechanistic
studies
suggest
that
the
process
initiated
by
energy
transfer
excited
photocatalyst
alkenes,
followed
single
electron
reduction,
protonation,
and
subsequent
oxidation
to
afford
key
alkyl
carbocation
intermediate.
This
protocol
exhibits
advantages
broad
functional
group
tolerance,
atom
economy,
efficiency,
mild
reaction
conditions.
We
herein
report
a
photochemical
Truce–Smiles
rearrangement
reaction
of
N-sulfinyl
acrylamides
with
bromodifluoroacetamides
resulting
in
the
synthesis
series
aryl
difluoroglutaramides
moderate
to
good
yields.
The
asymmetric
using
chiral
sulfinamides
produced
quaternary
carbon-centered
glutaramide
products
modest
enantioselectivity.
This
protocol
effectively
complements
previous
methods
involving
N-sulfonyl
acrylamides.