Chemical Communications,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Jan. 1, 2024
A
simple
cobalt-catalytic
aerobic
approach
for
the
direct
dithiolation
of
unactivated
alkenes
with
thiols
has
been
established,
enabling
efficient
access
to
symmetric
and
unsymmetric
vicinal
dithioethers
under
mild
reaction
conditions.
Chinese Journal of Chemistry,
Journal Year:
2024,
Volume and Issue:
42(22), P. 2751 - 2756
Published: July 12, 2024
Comprehensive
Summary
The
EDA
complex‐mediated
reactions
involving
oxime
esters
have
been
few
studied.
Herein,
an
complex
formed
by
thiophenolate
anion
and
ester
is
reported
for
photoinduced
divergent
synthesis
of
thioethers,
depending
on
different
types
esters.
Operational
simplicity,
mild
reaction
conditions,
flexible
options
leaving
group
demonstrate
the
generality
synthetic
utility
this
approach.
Such
approach
can
also
enable
interesting
thiol‐catalysis
phenanthridines.
The Journal of Organic Chemistry,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 3, 2025
A
hydropersulfide-mediated
hydrothiolation
reaction
of
alkenes
has
been
developed
for
C-S
bond
formation
with
Markovnikov
selectivity.
This
new
approach
is
a
transition-metal-,
additive-,
and
solvent-free
under
mild
conditions.
The
postulated
to
proceed
by
an
ionic
mechanism
the
release
elemental
sulfur
based
on
our
control
experiments
density
functional
theory
calculations.
Small,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 20, 2025
Abstract
Fabricating
visible‐light‐responsive
metal−organic
frameworks
(MOFs)
with
high
stability
and
effective
catalytic
functionality
remains
a
long‐term
pursuit
yet
great
challenge.
Herein,
strategy
of
increasing
ligand
cluster
connectivity
is
developed
to
construct
highly
stable
fluorescein
MOFs,
La‐CFL,
presenting
new
(4,8)‐connected
topological
structure
compared
Cd‐FL
constructed
using
6‐connected
dinuclear
clusters
3‐connected
tritopic
ligands.
La
8
(CFL)
4
containers
like
Chinese
“Ritual
Wine
Vessels
(Jue)”
resemble
linear
arrangements
interconnected
by
the
[La
2
(COO)
]
clusters.
This
arrangement
induces
benzene
rings
xanthene
locate
on
inner
walls
1D
channels,
resulting
in
thicker
channel
that
contribute
enhanced
stability.
Consequently,
La‐CFL
demonstrates
outstanding
performance
thiol–ene
reactions
under
green
LED
irradiation.
It
exhibits
2.3
times
higher
efficiency
than
while
reducing
reaction
time
one‐fifth
at
20
min.
Furthermore,
displays
size‐selective
catalysis
retains
full
activity
for
cycles
without
degradation,
an
improvement
over
Cd‐FL's
recyclability
limitations.
Organic Chemistry Frontiers,
Journal Year:
2024,
Volume and Issue:
11(11), P. 3131 - 3136
Published: Jan. 1, 2024
A
rapid
and
green
one-pot
access
to
S
-substituted
quaternary
carbon
centers
from
commercially
available
feedstock
chemicals
has
been
established,
providing
complex
molecules
with
high
chemoselectivity
by
the
use
of
air
as
terminal
oxidant.
Chemistry - An Asian Journal,
Journal Year:
2024,
Volume and Issue:
19(20)
Published: July 23, 2024
Abstract
A
very
simple
and
atom‐economical
method
for
the
synthesis
of
vicinal
trifluoromethyl
thioethers
via
DBN‐catalyzed
hydrothiolation
α‐(trifluoromethyl)styrenes
with
thiols
was
reported.
The
reaction
proceeded
smoothly
under
mild
conditions
provided
β‐CF
3
‐thioethers
in
moderate
to
good
yields
an
anti‐Markovnikov
manner.
Furthermore,
this
features
several
remarkable
advantages,
such
as
use
a
catalytic
amount
DBN,
broad
substrate
scope,
excellent
functional
group
compatibility,
easy
scalability.
Organic Letters,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Sept. 25, 2024
We
report
a
novel
cobalt-catalyzed
intramolecular
1,4-hydrofunctionalization
of
dienes.
The
reaction
proceeds
under
mild
conditions
and
is
amenable
to
N-
O-nucleophiles.
protocol
exhibits
exclusive
regioselectivity,
yielding
number
different
alkenyl
heterocycles,
including
but
not
limited
dihydroisobenzofurans,
isochromanes,
tetrahydrofurans,
morpholines,
lactones,
isoindolines.
Experimental
studies
were
performed
offer
some
insight
into
the
mechanistic
pathways
rationalize
regio-
stereoselectivities
reaction.