Recent Advances in Deoxygenative Thioether Synthesis Using Oxygenated Sulfur Surrogates
Synthesis,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 9, 2025
Abstract
Thioethers
(sulfides)
play
a
crucial
role
in
therapeutics,
diagnostics,
and
functional
materials.
Traditionally,
their
synthesis
involved
the
use
of
thiols
or
derivatives,
which
are
associated
with
unpleasant
odors
potential
health
risks.
Recently,
significant
research
has
focused
on
employing
oxygenated
sulfur
compounds,
such
as
sulfinates,
sulfonyl
oxyacids,
sulfoxides,
thiol
surrogates
for
thioether
synthesis.
This
review
highlights
recent
advancements
deoxygenative
synthesis,
categorizing
them
by
reaction
types,
including
cross-coupling
reactions,
C–H
functionalization,
hydro/halo/oxy-thiolation
unsaturated
hydrocarbons.
We
also
discuss
representative
mechanisms
to
provide
comprehensive
understanding
these
innovative
approaches.
1
Introduction
2
Cross-Coupling
Reactions
3
Functionalization
4
Hydro/Halo/Oxy-thiolation
Unsaturated
Hydrocarbons
5
Conclusion
Language: Английский
Na+ detection via brightening of synergistically originated noble metal nanoclusters
RSC Advances,
Journal Year:
2024,
Volume and Issue:
14(43), P. 31624 - 31632
Published: Jan. 1, 2024
Synergistically
originated
AuAg
nanoclusters
were
remarkably
brightened
in
the
presence
of
Na
+
.
Language: Английский
Synthesis of (E)‐β‐Iodovinyl Sulfones via HI‐mediated Vicinal Iodosulfonylation of Alkynes with Sodium Sulfinates
Zu‐Jia Chen,
No information about this author
Yu Zeng,
No information about this author
Zhonghao Li
No information about this author
et al.
Asian Journal of Organic Chemistry,
Journal Year:
2024,
Volume and Issue:
13(6)
Published: March 21, 2024
Abstract
Hydroiodic
acid‐mediated
vicinal
iodosulfonylation
reaction
of
alkynes
with
sodium
sulfinates
is
proposed
for
the
synthesis
(
E
)‐
β
‐iodovinyl
sulfones.
The
method
easy
to
operate,
environmentally
friendly,
using
inexpensive
and
easily
available
raw
materials,
giving
target
products
good
regio‐
stereoselectivity
in
satisfactory
yields.
Language: Английский
Iodine-Promoted Disproportionate Coupling Reaction of Arylsulfonyl Hydrazides: A Simple and Green Access to Thiosulfonates
Qi Chen,
No information about this author
Zhao-Hua Chen,
No information about this author
Shi‐Wei Yu
No information about this author
et al.
Synthesis,
Journal Year:
2024,
Volume and Issue:
56(09), P. 1415 - 1421
Published: Jan. 17, 2024
Abstract
An
environmentally
friendly
iodine-promoted
disproportionate
coupling
reaction
of
arylsulfonyl
hydrazides
is
reported.
This
strategy
can
synthesize
thiosulfonates
with
medium
to
excellent
yields,
and
features
a
green
system,
wide
applicability
substrates,
easy
availability
raw
materials.
The
preliminary
mechanistic
study
reveals
that
iodine
plays
an
important
role
in
the
radical
process.
Language: Английский
3,4-Dihalo-5-hydroxy-2(5H)-furanones: Highly Reactive Small Molecules
Molecules,
Journal Year:
2024,
Volume and Issue:
29(21), P. 5149 - 5149
Published: Oct. 31, 2024
3,4-Dichloro-5-hydroxy-2(5
Transition‐metal‐free Cyclization of Mucohalic Acids with Sulfonyl Hydrazides: An Approach to Pyridazin‐3(2H)‐ones
Asian Journal of Organic Chemistry,
Journal Year:
2023,
Volume and Issue:
12(11)
Published: Sept. 18, 2023
Abstract
An
eco‐friendly
and
efficient
synthesis
of
pyridazin‐3(2
H
)‐ones
from
aromatic
sulfonyl
hydrazides
mucohalic
acids
has
been
developed.
This
facile
strategy
is
carried
out
smoothly
via
the
promotion
simple
organic
acid
p
‐toluenesulfonic
acid,
able
to
form
two
C−N
bonds
a
heterocycle
linking
potentially
bioactive
group
at
one‐step.
The
protocol
tolerant
various
readily
available
substrates
in
good
yields,
as
desired
products
are
key
structural
fragments
many
compounds.
More
importantly,
gram‐scale
cyclization
reaction
novel
approach
derivatives
successfully
reveals
its
practicability.
Language: Английский