Electricity-driven, oxidative C–H selenylative and tellurylative annulation of N-(2-alkynyl)anilines: sustainable synthesis of 3-selanyl/tellanylquinolines
Chemical Communications,
Год журнала:
2024,
Номер
60(55), С. 7057 - 7060
Опубликована: Янв. 1, 2024
A
metal-
and
oxidant-free,
electricity-driven
C–H
selenylative
tellurylative
annulation
of
N
-(2-alkynyl)anilines
with
diorganyl
dichalcogenides
is
developed
to
access
3-chalcogenylquinolines.
Язык: Английский
Electrochemically Driven Chalcogenative Cyclization of 2-Alkynyl Aryl Oxime: Access to Functionalized Isoquinolines
The Journal of Organic Chemistry,
Год журнала:
2025,
Номер
unknown
Опубликована: Фев. 7, 2025
A
transition-metal-free
electrochemical
chalcogenative
cyclization
of
2-alkynyl
aryl
oxime
with
dichalcogenides
has
been
established
to
assemble
valuable
4-organochalcogen
isoquinolines
concisely.
This
protocol
proceeds
via
constant
electrolysis
in
a
user-friendly
undivided
cell
setup.
It
circumvents
the
necessity
transition
metal
catalysts,
chemical
oxidants,
and
harsh
reaction
conditions.
The
practical
utilities
current
were
illustrated
by
excellent
functional
group
tolerance,
remarkable
regio-selectivity,
easy
scalability,
mild
conditions,
transformable
isoquinoline
products.
Язык: Английский
Electrosynthesis of Highly Functionalized Quinolines through Radical Annulation–Polar Addition Cascade
Organic Letters,
Год журнала:
2024,
Номер
26(35), С. 7330 - 7335
Опубликована: Авг. 22, 2024
Synthesis
of
diversely
functionalized
quinoline-2-carboxylates
is
illustrated
through
electrochemical
cross-dehydrogenative
coupling
between
N-aryl
glycinates
and
methylenecyclopropanes.
An
extensive
range
distinct
functionalities
well-compatible
under
these
transition-metal-
oxidant-free
mild
conditions,
contributing
to
a
broad
substrate
scope
practical
applicability.
Cyclic
voltammetric
measurements
control
experiments
suggested
formal
[4
+
2]
cycloaddition
involving
radical
intermediates,
followed
by
cyclopropyl
ring
opening
nucleophilic
polar
addition,
consecutively
fabricating
C–C
C–N
bonds.
Язык: Английский
Tunable Electrochemical Diverse Sulfurization of Sulfoxonium Ylides with Disulfides
Chemical Communications,
Год журнала:
2024,
Номер
60(65), С. 8573 - 8576
Опубликована: Янв. 1, 2024
An
electrochemical
protocol
for
the
synthesis
of
sulfursulfoxonium
ylides
and
1,3-dithioketals
by
reacting
sulfoxonium
with
disulfides
has
been
developed
under
simple
mild
conditions.
By
changing
solubility
raw
materials
dielectric
parameters
electrolyte,
sulfurization
enabled
a
selective
dehydrogenation
C-S
construction
1,3-dithioketals.
The
transformation
is
an
ideal
approach
to
prepare
organosulfur
reagents
broad
functional
group
tolerance
as
well
high
selectivity,
which
leads
vicinal
difunctionalized
compounds.
Язык: Английский
Electrosynthesis of Cyclic Isoureas and Ureas Through Contiguous Heterofunctionalizations
The Journal of Organic Chemistry,
Год журнала:
2024,
Номер
89(16), С. 11323 - 11333
Опубликована: Июль 27, 2024
An
efficient
synthetic
protocol
for
the
selenylated
cyclic
isoureas
was
developed
using
electrochemical
activation
of
diselenides.
This
sustainable
approach
permitted
transition
metal
and
chemical
oxidant-free
difunctionalization
olefins
overall
access
to
distinct
1,2,3
triheterofunctionalized
carbon
skeletons.
Excellent
functional
group
tolerance
noticed,
allowing
synthesis
a
series
isourea
derivatives.
In
addition,
an
acid-triggered
skeletal
isomerization
facilitated
urea
derivatives
from
corresponding
isoureas.
Mechanistic
investigations,
along
with
voltammetric
studies,
enabled
postulation
reaction
mechanism.
Язык: Английский
Recent advances in electrochemically enabled construction of indoles
Chemical Communications,
Год журнала:
2024,
Номер
60(65), С. 8516 - 8525
Опубликована: Янв. 1, 2024
This
review
summarizes
recent
advances
in
the
electrochemically
enabled
construction
of
indoles
from
non-indole-based
precursors
and
their
underlying
mechanisms.
Язык: Английский
Total synthesis of bicyclomahanimbine by Cu(ii)-promoted photoredox process
RSC Advances,
Год журнала:
2024,
Номер
14(41), С. 30110 - 30115
Опубликована: Янв. 1, 2024
Since
the
isolation
of
carbazole
alkaloids,
synthetic
chemists
have
witnessed
an
upsurge
in
research
them
due
to
their
potential
pharmacological
properties.
Our
approach
shows
total
syntheses
five
such
biorelevant
pyrano-[3,2
Язык: Английский