The Journal of Organic Chemistry,
Год журнала:
2024,
Номер
unknown
Опубликована: Дек. 23, 2024
6/5/3-Fused
tricyclic
enones
were
obtained
when
4-(alkynyloxy)cyclohexa-2,5-dienones
treated
with
DMSO
at
150
°C.
The
reaction
proceeded
via
a
four-membered
oxathietene
intermediate.
protocol
developed
is
atom
economical,
has
broad
substrate
scope,
and
amenable
to
gram-scale
synthesis.
products
are
susceptible
further
synthetic
transformations.
Environmental Science & Technology,
Год журнала:
2024,
Номер
unknown
Опубликована: Ноя. 19, 2024
The
recently
proposed
partial
denitrification
(PD),
terminating
nitrate
reduction
to
nitrite,
has
been
regarded
as
a
promising
alternative
nitrite
supplying
for
anammox
bacteria.
most
important
aspect
of
the
PD
process
engineering
application
is
stable
and
continuous
supply
nitrite.
However,
activity
reductase
often
higher
than
that
(NIR),
making
it
difficult
accumulate
during
process.
Herein,
strategy
achieving
efficient
using
biosafe
additive
dimethyl
sulfoxide
(DMSO)
was
constructed,
mechanism
DMSO
inhibiting
NIR
analyzed.
addition
reduced
expression
gene,
1%
can
significantly
inhibit
enzyme
achieve
When
concentration
increased
3.5%,
almost
inhibited
with
only
0.95
mg
nitrite/min.
no
inhibitory
effect
on
(NAR)
enzyme.
affinity
constant
NAR
−2.4
kcal/mol,
while
high
−3.1
kcal/mol.
shows
NIR.
Moreover,
occupy
same
catalytic
cavity
in
enzyme,
which
fundamental
reason
why
selectively
inhibits
This
study
provides
new
idea
realizing
function.
Chemical Communications,
Год журнала:
2023,
Номер
59(36), С. 5343 - 5364
Опубликована: Янв. 1, 2023
The
activation
and
transformation
of
organic
chemical
bonds
is
a
fundamental
scientific
problem.
In
the
past
several
decades,
C-S
bond
cleavage
for
construction
C-C
C-heteroatom
has
received
tremendous
attention
in
chemistry.
Although
significant
progress
been
made
field
transition
metal
strategies,
variety
novel
transition-metal-free
strategies
have
also
developed
using
halogenated
reagents,
oxidants,
acids,
bases.
Moreover,
photochemical
electrochemical
methods
to
achieve
organosulfur
compounds.
To
date,
however,
no
comprehensive
review
reported.
Therefore,
we
herein
provide
major
advances
compounds,
including
thioethers,
sulfoxides,
sulfones,
thioacetals,
sulfonium
salts,
sulfur
ylides.
Chinese Journal of Chemistry,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 16, 2025
Comprehensive
Summary
The
N–H
methylsulfoxidation
of
sulfoximines
using
DMSO
as
a
methylsulfinyl
source,
induced
by
electrochemistry,
has
been
developed.
This
method
is
the
first
example
an
electrochemical
reaction
in
which
serves
source.
Unlike
previous
reactions
involving
substrate,
exclusively
proceed
via
radical
mechanisms,
this
follows
S‐cation
pathway.
A
wide
range
N
‐methylsulfinyl
were
successfully
obtained.
KOtBu-promoted
[3
+
2]
cycloaddition
of
dimethyl
sulfoxide
(DMSO)
with
fullerenes
has
been
developed
for
facile
and
efficient
one-pot
synthesis
1,2,3,4-cyclic
sulfoxide-fused
[60]/[70]fullerene
dihydrides,
which
offers
a
versatile
platform
the
site-selective
preparation
various
fullerene
multiadducts
wide
range
functional
groups.
The
utility
these
tetra-functionalized
is
demonstrated
by
successful
application
as
electron-transport
materials
in
perovskite
solar
cells.
RSC Advances,
Год журнала:
2025,
Номер
15(11), С. 8750 - 8756
Опубликована: Янв. 1, 2025
An
efficient
and
convenient
protocol
for
copper-promoted
oxidative
mono-
di-bromination
of
8-aminoquinoline
amides
using
hydrogen
bromide
(HBr)
as
the
brominating
reagent
dimethyl
sulfoxide
(DMSO)
a
mild
oxidant
has
been
developed.
The Journal of Organic Chemistry,
Год журнала:
2025,
Номер
unknown
Опубликована: Апрель 10, 2025
An
efficient
and
attractive
method
for
the
synthesis
of
valuable
benzofuran-3(2H)-one
derivatives
bearing
a
quaternary
center
in
one
step
by
employing
dimethyl
sulfoxide
(DMSO)
as
dual
synthon
under
metal-free
conditions
has
been
developed.
In
this
reaction,
DMSO
activated
cyanuric
chloride
(TCT)
provides
two
different
units
(CH3
SMe)
target
molecules,
construction
carbon
benzofuran-3(2H)-ones
can
be
controlled
addition
water.
Furthermore,
functional
group
compatibility
synthetic
value
were
demonstrated
scope
evaluation
gram-scale
experiments.
The
mechanistic
studies
show
that
reaction
may
proceed
via
radical
process.