Organic Chemistry Frontiers,
Journal Year:
2024,
Volume and Issue:
11(9), P. 2566 - 2571
Published: Jan. 1, 2024
A
general,
efficient,
and
mild
Dha
electrochemical
modification
strategy
is
reported,
which
enables
a
divergent
route
to
various
α,α-disubstituted
amino
esters
via
anodic
cascade
oxidation
nucleophilic
attack.
Green Chemistry,
Journal Year:
2024,
Volume and Issue:
26(6), P. 3435 - 3440
Published: Jan. 1, 2024
A
practical
electrosynthesis
of
aryl
sulfonyl
fluorides
from
nitroarenes
is
described.
Cheap
N
-methylimidazolium
p
-toluenesulfonate
has
been
found
to
be
an
effective
additive,
promoting
the
desired
fluorosulfonylation
under
very
mild
conditions.
Organic Letters,
Journal Year:
2023,
Volume and Issue:
26(1), P. 411 - 415
Published: Dec. 26, 2023
We
report
a
strategic
exploitation
of
trifluoromethyl
thianthrenium
triflate
(TT-CF3+OTf–)
as
both
electromediator
and
CF3
radical
precursors
for
paired
electrolysis.
Enabled
by
this
strategy,
the
three-component
trifluoromethylheteroaromatization
alkenes
alkynes
was
realized.
The
superiority
TT-CF3+OTf–
to
other
electrophilic
reagents
is
attributed
cathodic
generation
thianthrene
(TT)
mediator,
which
shifts
heterogeneous
oxidation
interest
homogeneous
one.
Chinese Journal of Chemistry,
Journal Year:
2024,
Volume and Issue:
42(15), P. 1691 - 1698
Published: March 19, 2024
Comprehensive
Summary
A
novel
electrochemical
multicomponent
cascade
reaction
of
indole‐tethered
alkenes
with
CF
3
SO
2
Na
and
n
‐Bu
4
NI
has
been
developed,
which
enables
the
rapid
assembly
spiropyrrolidinyl‐oxindoles
in
good
yields.
The
experimental
results
DFT
calculations
suggest
that
this
proceeds
through
oxidation
Na,
radical
coupling
alkene,
spirocyclization,
sulfinate,
iodide
substitution,
water
coupling.
This
strategy
features
mild
conditions,
easy‐to‐handle
reactants,
chemical
finding
not
only
enriches
research
contents
but
also
provides
a
green
for
construction
compared
existing
methodologies.
Organic Letters,
Journal Year:
2024,
Volume and Issue:
26(2), P. 493 - 497
Published: Jan. 8, 2024
An
electrochemical
hydrogen
atom
transfer
(HAT)
strategy
for
the
direct
amino-α-C–H
heteroarylation
of
amides
is
described.
The
cheap
TMSN3
acts
as
a
reagent.
A
series
heteroarenes
including
quinoxalin-2(1H)-ones,
4-methylquinoline,
isoquinoline,
2-methylquinoxaline,
benzothiazole,
etc.,
and
various
readily
available
amides/lactams
were
suitable.
reaction
has
characteristics
wide
range
substrates,
good
regioselectivity,
chemical
oxidant-free
conditions,
etc.
The Chemical Record,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 3, 2025
Abstract
Owing
to
their
wide
utilizations
in
synthesis
and
products
prevalence
numerous
natural
products,
pharmaceuticals
functional
materials,
the
alkene
difunctionalization
methods
for
selective
transformations
of
olefins
are
important
have
attracted
much
attention
form
synthetic
chemists.
Among
them,
electrochemical
reaction
is
particularly
promising
has
becoming
a
potent
sustainable
tool
alkenes
into
vicinal
difunctionalized
structures
organic
through
simultaneous
incorporation
two
groups.
Herein,
we
summarize
recent
progress
reactions
according
types
as
well
category
radicals
over
past
five
years.
By
selecting
remarkable
examples,
elaborately
discussed
substrate
scope
mechanisms
olefin
reaction.
Organic Chemistry Frontiers,
Journal Year:
2024,
Volume and Issue:
11(8), P. 2283 - 2288
Published: Jan. 1, 2024
An
electrochemical
thiocyanation
of
distal
C(sp
3
)–H
bonds
based
on
amidyl
radical-mediated
1,5-HAT
has
been
developed.
The
transformation
is
highly
site-selective
and
compatible
with
primary,
secondary,
tertiary
sulfonamides,
bioactive
derivatives.